Canonical Allele Identifier: CA369588878
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711080
ClinVar RCV Id: RCV002292367
dbSNP Id: rs1586140512

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781600T>C , CM000669.2:g.140781600T>C GRCh38
NC_000007.13:g.140481400T>C , CM000669.1:g.140481400T>C GRCh37
NC_000007.12:g.140127869T>C NCBI36
NG_007873.3:g.148165A>G , LRG_299:g.148165A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1408A>G MANE Select ENSP00000493543.1:p.Thr470Ala
ENST00000288602.11:c.1528A>G ENSP00000288602.7:p.Thr510Ala
ENST00000479537.6:c.78A>G
ENST00000496384.7:c.1408A>G ENSP00000419060.2:p.Thr470Ala
ENST00000497784.2:c.*858A>G ENSP00000420119.2:n.*858A>G
ENST00000642228.1:c.*486A>G ENSP00000493678.1:n.*486A>G
ENST00000642875.1:n.850A>G
ENST00000644120.1:n.1798A>G
ENST00000644650.1:c.504A>G
ENST00000644905.1:n.1497A>G
ENST00000644969.2:c.1528A>G MANE Plus Clinical ENSP00000496776.1:p.Thr510Ala
ENST00000646334.1:n.538A>G
ENST00000646730.1:c.1408A>G ENSP00000494784.1:p.Thr470Ala
ENST00000646891.1:c.1408A>G ENSP00000493543.1:p.Thr470Ala
ENST00000647434.1:c.451A>G ENSP00000495132.1:p.Thr151Ala
ENST00000288602.10:c.1408A>G ENSP00000288602.6:p.Thr470Ala
ENST00000496384.6:c.231A>G
ENST00000497784.1:c.1443A>G ENSP00000420119.1:n.1443A>G
NM_004333.4:c.1408A>G , LRG_299t1:c.1408A>G NP_004324.2:p.Thr470Ala
XM_005250045.1:c.1408A>G XP_005250102.1:p.Thr470Ala
XM_005250046.1:c.1408A>G XP_005250103.1:p.Thr470Ala
XM_011516529.1:c.1408A>G XP_011514831.1:p.Thr470Ala
XM_011516530.1:c.1408A>G XP_011514832.1:p.Thr470Ala
XR_242190.1:n.1416A>G
XR_927520.1:n.1416A>G
XR_927521.1:n.1416A>G
XR_927522.1:n.1416A>G
XR_927523.1:n.1416A>G
NM_001354609.1:c.1408A>G NP_001341538.1:p.Thr470Ala
NM_004333.5:c.1408A>G NP_004324.2:p.Thr470Ala
NR_148928.1:n.1713A>G
XM_017012558.1:c.1528A>G XP_016868047.1:p.Thr510Ala
XM_017012559.1:c.1528A>G XP_016868048.1:p.Thr510Ala
XR_001744857.1:n.1536A>G
XR_001744858.1:n.1536A>G
NM_001354609.2:c.1408A>G NP_001341538.1:p.Thr470Ala
NM_001374244.1:c.1528A>G NP_001361173.1:p.Thr510Ala
NM_001374258.1:c.1528A>G MANE Plus Clinical NP_001361187.1:p.Thr510Ala
NM_004333.6:c.1408A>G MANE Select NP_004324.2:p.Thr470Ala
NM_001378467.1:c.1417A>G NP_001365396.1:p.Thr473Ala
NM_001378468.1:c.1408A>G NP_001365397.1:p.Thr470Ala
NM_001378469.1:c.1342A>G NP_001365398.1:p.Thr448Ala
NM_001378470.1:c.1306A>G NP_001365399.1:p.Thr436Ala
NM_001378471.1:c.1297A>G NP_001365400.1:p.Thr433Ala
NM_001378472.1:c.1252A>G NP_001365401.1:p.Thr418Ala
NM_001378473.1:c.1252A>G NP_001365402.1:p.Thr418Ala
NM_001378474.1:c.1408A>G NP_001365403.1:p.Thr470Ala
NM_001378475.1:c.1144A>G NP_001365404.1:p.Thr382Ala