Canonical Allele Identifier: CA1747732059
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140800385G= , CM000669.2:g.140800385G= GRCh38
NC_000007.13:g.140500185G= , CM000669.1:g.140500185G= GRCh37
NC_000007.12:g.140146654G= NCBI36
NG_007873.3:g.129380C= , LRG_299:g.129380C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.957C= MANE Select ENSP00000493543.1:p.Ser319=
ENST00000288602.11:c.957C= ENSP00000288602.7:p.Ser319=
ENST00000496384.7:c.957C= ENSP00000419060.2:p.Ser319=
ENST00000497784.2:c.*407C= ENSP00000420119.2:n.*407C=
ENST00000642228.1:c.*35C= ENSP00000493678.1:n.*35C=
ENST00000642272.1:n.989C=
ENST00000642875.1:n.451C=
ENST00000644120.1:n.1399C=
ENST00000644650.1:c.53C=
ENST00000644905.1:n.1046C=
ENST00000644969.2:c.957C= MANE Plus Clinical ENSP00000496776.1:p.Ser319=
ENST00000646730.1:c.957C= ENSP00000494784.1:p.Ser319=
ENST00000646891.1:c.957C= ENSP00000493543.1:p.Ser319=
ENST00000288602.10:c.957C= ENSP00000288602.6:p.Ser319=
ENST00000497784.1:c.992C= ENSP00000420119.1:n.992C=
NM_004333.4:c.957C= , LRG_299t1:c.957C= NP_004324.2:p.Ser319=
XM_005250045.1:c.957C= XP_005250102.1:p.Ser319=
XM_005250046.1:c.957C= XP_005250103.1:p.Ser319=
XM_011516529.1:c.957C= XP_011514831.1:p.Ser319=
XM_011516530.1:c.957C= XP_011514832.1:p.Ser319=
XR_242190.1:n.965C=
XR_927520.1:n.965C=
XR_927521.1:n.965C=
XR_927522.1:n.965C=
XR_927523.1:n.965C=
NM_001354609.1:c.957C= NP_001341538.1:p.Ser319=
NM_004333.5:c.957C= NP_004324.2:p.Ser319=
NR_148928.1:n.1262C=
XM_017012558.1:c.957C= XP_016868047.1:p.Ser319=
XM_017012559.1:c.957C= XP_016868048.1:p.Ser319=
XR_001744857.1:n.965C=
XR_001744858.1:n.965C=
NM_001354609.2:c.957C= NP_001341538.1:p.Ser319=
NM_001374244.1:c.957C= NP_001361173.1:p.Ser319=
NM_001374258.1:c.957C= MANE Plus Clinical NP_001361187.1:p.Ser319=
NM_004333.6:c.957C= MANE Select NP_004324.2:p.Ser319=
NM_001378467.1:c.966C= NP_001365396.1:p.Ser322=
NM_001378468.1:c.957C= NP_001365397.1:p.Ser319=
NM_001378469.1:c.957C= NP_001365398.1:p.Ser319=
NM_001378470.1:c.855C= NP_001365399.1:p.Ser285=
NM_001378471.1:c.957C= NP_001365400.1:p.Ser319=
NM_001378472.1:c.801C= NP_001365401.1:p.Ser267=
NM_001378473.1:c.801C= NP_001365402.1:p.Ser267=
NM_001378474.1:c.957C= NP_001365403.1:p.Ser319=
NM_001378475.1:c.693C= NP_001365404.1:p.Ser231=