Canonical Allele Identifier: CA2695199640
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 2664272
ClinVar RCV Id: RCV003445403

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753325_140753336delinsCAT , CM000669.2:g.140753325_140753336delinsCAT GRCh38
NC_000007.13:g.140453125_140453136delinsCAT , CM000669.1:g.140453125_140453136delinsCAT GRCh37
NC_000007.12:g.140099594_140099605delinsCAT NCBI36
NG_007873.3:g.176429_176440delinsATG , LRG_299:g.176429_176440delinsATG

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1799_1810delinsATG MANE Select ENSP00000493543.1:p.Val600_Trp604delinsAs...
ENST00000288602.11:c.1919_1930delinsATG ENSP00000288602.7:p.Val640_Trp644delinsAs...
ENST00000479537.6:c.469_480delinsATG
ENST00000496384.7:c.1799_1810delinsATG ENSP00000419060.2:p.Val600_Trp604delinsAs...
ENST00000497784.2:c.*1249_*1260delinsATG ENSP00000420119.2:n.*1249_*1260delinsATG
ENST00000642228.1:c.*877_*888delinsATG ENSP00000493678.1:n.*877_*888delinsATG
ENST00000642875.1:n.1259-3918_1259-3907delinsATG
ENST00000644120.1:n.2189_2200delinsATG
ENST00000644650.1:c.895_906delinsATG
ENST00000644905.1:n.2681_2692delinsATG
ENST00000644969.2:c.1919_1930delinsATG MANE Plus Clinical ENSP00000496776.1:p.Val640_Trp644delinsAs...
ENST00000646730.1:c.*375_*386delinsATG ENSP00000494784.1:n.*375_*386delinsATG
ENST00000646891.1:c.1799_1810delinsATG ENSP00000493543.1:p.Val600_Trp604delinsAs...
ENST00000647434.1:c.738-3918_738-3907delinsATG ENSP00000495132.1:n.738-3918_738-3907deli...
ENST00000288602.10:c.1799_1810delinsATG ENSP00000288602.6:p.Val600_Trp604delinsAs...
ENST00000479537.5:c.83_94delinsATG ENSP00000418033.1:p.Val28_Trp32delinsAspG...
ENST00000496384.6:c.622_633delinsATG
ENST00000497784.1:c.1834_1845delinsATG ENSP00000420119.1:n.1834_1845delinsATG
NM_004333.4:c.1799_1810delinsATG , LRG_299t1:c.1799_1810delinsATG NP_004324.2:p.Val600_Trp604delinsAspGly
XM_005250045.1:c.1799_1810delinsATG XP_005250102.1:p.Val600_Trp604delinsAspGl...
XM_005250046.1:c.1799_1810delinsATG XP_005250103.1:p.Val600_Trp604delinsAspGl...
XM_011516529.1:c.1799_1810delinsATG XP_011514831.1:p.Val600_Trp604delinsAspGl...
XM_011516530.1:c.1695-3918_1695-3907delinsATG XP_011514832.1:n.1695-3918_1695-3907delin...
XR_242190.1:n.1807_1818delinsATG
XR_927520.1:n.1807_1818delinsATG
XR_927521.1:n.1807_1818delinsATG
XR_927522.1:n.1703-3918_1703-3907delinsATG
XR_927523.1:n.1703-3918_1703-3907delinsATG
NM_001354609.1:c.1799_1810delinsATG NP_001341538.1:p.Val600_Trp604delinsAspGl...
NM_004333.5:c.1799_1810delinsATG NP_004324.2:p.Val600_Trp604delinsAspGly
NR_148928.1:n.2897_2908delinsATG
XM_017012558.1:c.1919_1930delinsATG XP_016868047.1:p.Val640_Trp644delinsAspGl...
XM_017012559.1:c.1919_1930delinsATG XP_016868048.1:p.Val640_Trp644delinsAspGl...
XR_001744857.1:n.1927_1938delinsATG
XR_001744858.1:n.1823-3918_1823-3907delinsATG
NM_001354609.2:c.1799_1810delinsATG NP_001341538.1:p.Val600_Trp604delinsAspGl...
NM_001374244.1:c.1919_1930delinsATG NP_001361173.1:p.Val640_Trp644delinsAspGl...
NM_001374258.1:c.1919_1930delinsATG MANE Plus Clinical NP_001361187.1:p.Val640_Trp644delinsAspGl...
NM_004333.6:c.1799_1810delinsATG MANE Select NP_004324.2:p.Val600_Trp604delinsAspGly
NM_001378467.1:c.1808_1819delinsATG NP_001365396.1:p.Val603_Trp607delinsAspGl...
NM_001378468.1:c.1799_1810delinsATG NP_001365397.1:p.Val600_Trp604delinsAspGl...
NM_001378469.1:c.1733_1744delinsATG NP_001365398.1:p.Val578_Trp582delinsAspGl...
NM_001378470.1:c.1697_1708delinsATG NP_001365399.1:p.Val566_Trp570delinsAspGl...
NM_001378471.1:c.1688_1699delinsATG NP_001365400.1:p.Val563_Trp567delinsAspGl...
NM_001378472.1:c.1643_1654delinsATG NP_001365401.1:p.Val548_Trp552delinsAspGl...
NM_001378473.1:c.1643_1654delinsATG NP_001365402.1:p.Val548_Trp552delinsAspGl...
NM_001378474.1:c.1799_1810delinsATG NP_001365403.1:p.Val600_Trp604delinsAspGl...
NM_001378475.1:c.1535_1546delinsATG NP_001365404.1:p.Val512_Trp516delinsAspGl...