Canonical Allele Identifier: CA458115977
Gene: BRAF HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.140481485A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781685A>G , CM000669.2:g.140781685A>G GRCh38
NC_000007.13:g.140481485A>G , CM000669.1:g.140481485A>G GRCh37
NC_000007.12:g.140127954A>G NCBI36
NG_007873.3:g.148080T>C , LRG_299:g.148080T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1323T>C MANE Select ENSP00000493543.1:p.Leu441=
ENST00000288602.11:c.1443T>C ENSP00000288602.7:p.Leu481=
ENST00000496384.7:c.1323T>C ENSP00000419060.2:p.Leu441=
ENST00000497784.2:c.*773T>C ENSP00000420119.2:n.*773T>C
ENST00000642228.1:c.*401T>C ENSP00000493678.1:n.*401T>C
ENST00000642875.1:n.765T>C
ENST00000644120.1:n.1713T>C
ENST00000644650.1:c.419T>C
ENST00000644905.1:n.1412T>C
ENST00000644969.2:c.1443T>C MANE Plus Clinical ENSP00000496776.1:p.Leu481=
ENST00000646334.1:n.453T>C
ENST00000646730.1:c.1323T>C ENSP00000494784.1:p.Leu441=
ENST00000646891.1:c.1323T>C ENSP00000493543.1:p.Leu441=
ENST00000647434.1:c.366T>C ENSP00000495132.1:p.Leu122=
ENST00000288602.10:c.1323T>C ENSP00000288602.6:p.Leu441=
ENST00000496384.6:c.146T>C
ENST00000497784.1:c.1358T>C ENSP00000420119.1:n.1358T>C
NM_004333.4:c.1323T>C , LRG_299t1:c.1323T>C NP_004324.2:p.Leu441=
XM_005250045.1:c.1323T>C XP_005250102.1:p.Leu441=
XM_005250046.1:c.1323T>C XP_005250103.1:p.Leu441=
XM_011516529.1:c.1323T>C XP_011514831.1:p.Leu441=
XM_011516530.1:c.1323T>C XP_011514832.1:p.Leu441=
XR_242190.1:n.1331T>C
XR_927520.1:n.1331T>C
XR_927521.1:n.1331T>C
XR_927522.1:n.1331T>C
XR_927523.1:n.1331T>C
NM_001354609.1:c.1323T>C NP_001341538.1:p.Leu441=
NM_004333.5:c.1323T>C NP_004324.2:p.Leu441=
NR_148928.1:n.1628T>C
XM_017012558.1:c.1443T>C XP_016868047.1:p.Leu481=
XM_017012559.1:c.1443T>C XP_016868048.1:p.Leu481=
XR_001744857.1:n.1451T>C
XR_001744858.1:n.1451T>C
NM_001354609.2:c.1323T>C NP_001341538.1:p.Leu441=
NM_001374244.1:c.1443T>C NP_001361173.1:p.Leu481=
NM_001374258.1:c.1443T>C MANE Plus Clinical NP_001361187.1:p.Leu481=
NM_004333.6:c.1323T>C MANE Select NP_004324.2:p.Leu441=
NM_001378467.1:c.1332T>C NP_001365396.1:p.Leu444=
NM_001378468.1:c.1323T>C NP_001365397.1:p.Leu441=
NM_001378469.1:c.1257T>C NP_001365398.1:p.Leu419=
NM_001378470.1:c.1221T>C NP_001365399.1:p.Leu407=
NM_001378471.1:c.1212T>C NP_001365400.1:p.Leu404=
NM_001378472.1:c.1167T>C NP_001365401.1:p.Leu389=
NM_001378473.1:c.1167T>C NP_001365402.1:p.Leu389=
NM_001378474.1:c.1323T>C NP_001365403.1:p.Leu441=
NM_001378475.1:c.1059T>C NP_001365404.1:p.Leu353=