Canonical Allele Identifier: CA369589050
Gene: BRAF HGNC NCBI

Linked Data

dbSNP Id: rs2129023979

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781687G>C , CM000669.2:g.140781687G>C GRCh38
NC_000007.13:g.140481487G>C , CM000669.1:g.140481487G>C GRCh37
NC_000007.12:g.140127956G>C NCBI36
NG_007873.3:g.148078C>G , LRG_299:g.148078C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1321C>G MANE Select ENSP00000493543.1:p.Leu441Val
ENST00000288602.11:c.1441C>G ENSP00000288602.7:p.Leu481Val
ENST00000496384.7:c.1321C>G ENSP00000419060.2:p.Leu441Val
ENST00000497784.2:c.*771C>G ENSP00000420119.2:n.*771C>G
ENST00000642228.1:c.*399C>G ENSP00000493678.1:n.*399C>G
ENST00000642875.1:n.763C>G
ENST00000644120.1:n.1711C>G
ENST00000644650.1:c.417C>G
ENST00000644905.1:n.1410C>G
ENST00000644969.2:c.1441C>G MANE Plus Clinical ENSP00000496776.1:p.Leu481Val
ENST00000646334.1:n.451C>G
ENST00000646730.1:c.1321C>G ENSP00000494784.1:p.Leu441Val
ENST00000646891.1:c.1321C>G ENSP00000493543.1:p.Leu441Val
ENST00000647434.1:c.364C>G ENSP00000495132.1:p.Leu122Val
ENST00000288602.10:c.1321C>G ENSP00000288602.6:p.Leu441Val
ENST00000496384.6:c.144C>G
ENST00000497784.1:c.1356C>G ENSP00000420119.1:n.1356C>G
NM_004333.4:c.1321C>G , LRG_299t1:c.1321C>G NP_004324.2:p.Leu441Val
XM_005250045.1:c.1321C>G XP_005250102.1:p.Leu441Val
XM_005250046.1:c.1321C>G XP_005250103.1:p.Leu441Val
XM_011516529.1:c.1321C>G XP_011514831.1:p.Leu441Val
XM_011516530.1:c.1321C>G XP_011514832.1:p.Leu441Val
XR_242190.1:n.1329C>G
XR_927520.1:n.1329C>G
XR_927521.1:n.1329C>G
XR_927522.1:n.1329C>G
XR_927523.1:n.1329C>G
NM_001354609.1:c.1321C>G NP_001341538.1:p.Leu441Val
NM_004333.5:c.1321C>G NP_004324.2:p.Leu441Val
NR_148928.1:n.1626C>G
XM_017012558.1:c.1441C>G XP_016868047.1:p.Leu481Val
XM_017012559.1:c.1441C>G XP_016868048.1:p.Leu481Val
XR_001744857.1:n.1449C>G
XR_001744858.1:n.1449C>G
NM_001354609.2:c.1321C>G NP_001341538.1:p.Leu441Val
NM_001374244.1:c.1441C>G NP_001361173.1:p.Leu481Val
NM_001374258.1:c.1441C>G MANE Plus Clinical NP_001361187.1:p.Leu481Val
NM_004333.6:c.1321C>G MANE Select NP_004324.2:p.Leu441Val
NM_001378467.1:c.1330C>G NP_001365396.1:p.Leu444Val
NM_001378468.1:c.1321C>G NP_001365397.1:p.Leu441Val
NM_001378469.1:c.1255C>G NP_001365398.1:p.Leu419Val
NM_001378470.1:c.1219C>G NP_001365399.1:p.Leu407Val
NM_001378471.1:c.1210C>G NP_001365400.1:p.Leu404Val
NM_001378472.1:c.1165C>G NP_001365401.1:p.Leu389Val
NM_001378473.1:c.1165C>G NP_001365402.1:p.Leu389Val
NM_001378474.1:c.1321C>G NP_001365403.1:p.Leu441Val
NM_001378475.1:c.1057C>G NP_001365404.1:p.Leu353Val