Canonical Allele Identifier: CA369588823
Gene: BRAF HGNC NCBI

Linked Data

dbSNP Id: rs1439898547

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781577A>T , CM000669.2:g.140781577A>T GRCh38
NC_000007.13:g.140481377A>T , CM000669.1:g.140481377A>T GRCh37
NC_000007.12:g.140127846A>T NCBI36
NG_007873.3:g.148188T>A , LRG_299:g.148188T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1431T>A MANE Select ENSP00000493543.1:p.His477Gln
ENST00000288602.11:c.1551T>A ENSP00000288602.7:p.His517Gln
ENST00000479537.6:c.101T>A
ENST00000496384.7:c.1431T>A ENSP00000419060.2:p.His477Gln
ENST00000497784.2:c.*881T>A ENSP00000420119.2:n.*881T>A
ENST00000642228.1:c.*509T>A ENSP00000493678.1:n.*509T>A
ENST00000642875.1:n.873T>A
ENST00000644120.1:n.1821T>A
ENST00000644650.1:c.527T>A
ENST00000644905.1:n.1520T>A
ENST00000644969.2:c.1551T>A MANE Plus Clinical ENSP00000496776.1:p.His517Gln
ENST00000646334.1:n.561T>A
ENST00000646730.1:c.1431T>A ENSP00000494784.1:p.His477Gln
ENST00000646891.1:c.1431T>A ENSP00000493543.1:p.His477Gln
ENST00000647434.1:c.474T>A ENSP00000495132.1:p.His158Gln
ENST00000288602.10:c.1431T>A ENSP00000288602.6:p.His477Gln
ENST00000496384.6:c.254T>A
ENST00000497784.1:c.1466T>A ENSP00000420119.1:n.1466T>A
NM_004333.4:c.1431T>A , LRG_299t1:c.1431T>A NP_004324.2:p.His477Gln
XM_005250045.1:c.1431T>A XP_005250102.1:p.His477Gln
XM_005250046.1:c.1431T>A XP_005250103.1:p.His477Gln
XM_011516529.1:c.1431T>A XP_011514831.1:p.His477Gln
XM_011516530.1:c.1431T>A XP_011514832.1:p.His477Gln
XR_242190.1:n.1439T>A
XR_927520.1:n.1439T>A
XR_927521.1:n.1439T>A
XR_927522.1:n.1439T>A
XR_927523.1:n.1439T>A
NM_001354609.1:c.1431T>A NP_001341538.1:p.His477Gln
NM_004333.5:c.1431T>A NP_004324.2:p.His477Gln
NR_148928.1:n.1736T>A
XM_017012558.1:c.1551T>A XP_016868047.1:p.His517Gln
XM_017012559.1:c.1551T>A XP_016868048.1:p.His517Gln
XR_001744857.1:n.1559T>A
XR_001744858.1:n.1559T>A
NM_001354609.2:c.1431T>A NP_001341538.1:p.His477Gln
NM_001374244.1:c.1551T>A NP_001361173.1:p.His517Gln
NM_001374258.1:c.1551T>A MANE Plus Clinical NP_001361187.1:p.His517Gln
NM_004333.6:c.1431T>A MANE Select NP_004324.2:p.His477Gln
NM_001378467.1:c.1440T>A NP_001365396.1:p.His480Gln
NM_001378468.1:c.1431T>A NP_001365397.1:p.His477Gln
NM_001378469.1:c.1365T>A NP_001365398.1:p.His455Gln
NM_001378470.1:c.1329T>A NP_001365399.1:p.His443Gln
NM_001378471.1:c.1320T>A NP_001365400.1:p.His440Gln
NM_001378472.1:c.1275T>A NP_001365401.1:p.His425Gln
NM_001378473.1:c.1275T>A NP_001365402.1:p.His425Gln
NM_001378474.1:c.1431T>A NP_001365403.1:p.His477Gln
NM_001378475.1:c.1167T>A NP_001365404.1:p.His389Gln