Canonical Allele Identifier: CA1747709995
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753323C= , CM000669.2:g.140753323C= GRCh38
NC_000007.13:g.140453123C= , CM000669.1:g.140453123C= GRCh37
NC_000007.12:g.140099592C= NCBI36
NG_007873.3:g.176442G= , LRG_299:g.176442G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1812G= MANE Select ENSP00000493543.1:p.Trp604=
ENST00000288602.11:c.1932G= ENSP00000288602.7:p.Trp644=
ENST00000479537.6:c.482G=
ENST00000496384.7:c.1812G= ENSP00000419060.2:p.Trp604=
ENST00000497784.2:c.*1262G= ENSP00000420119.2:n.*1262G=
ENST00000642228.1:c.*890G= ENSP00000493678.1:n.*890G=
ENST00000642875.1:n.1259-3905G=
ENST00000644120.1:n.2202G=
ENST00000644650.1:c.908G=
ENST00000644905.1:n.2694G=
ENST00000644969.2:c.1932G= MANE Plus Clinical ENSP00000496776.1:p.Trp644=
ENST00000646730.1:c.*388G= ENSP00000494784.1:n.*388G=
ENST00000646891.1:c.1812G= ENSP00000493543.1:p.Trp604=
ENST00000647434.1:c.738-3905G= ENSP00000495132.1:n.738-3905G=
ENST00000288602.10:c.1812G= ENSP00000288602.6:p.Trp604=
ENST00000479537.5:c.96G= ENSP00000418033.1:p.Trp32=
ENST00000496384.6:c.635G=
ENST00000497784.1:c.1847G= ENSP00000420119.1:n.1847G=
NM_004333.4:c.1812G= , LRG_299t1:c.1812G= NP_004324.2:p.Trp604=
XM_005250045.1:c.1812G= XP_005250102.1:p.Trp604=
XM_005250046.1:c.1812G= XP_005250103.1:p.Trp604=
XM_011516529.1:c.1812G= XP_011514831.1:p.Trp604=
XM_011516530.1:c.1695-3905G= XP_011514832.1:n.1695-3905G=
XR_242190.1:n.1820G=
XR_927520.1:n.1820G=
XR_927521.1:n.1820G=
XR_927522.1:n.1703-3905G=
XR_927523.1:n.1703-3905G=
NM_001354609.1:c.1812G= NP_001341538.1:p.Trp604=
NM_004333.5:c.1812G= NP_004324.2:p.Trp604=
NR_148928.1:n.2910G=
XM_017012558.1:c.1932G= XP_016868047.1:p.Trp644=
XM_017012559.1:c.1932G= XP_016868048.1:p.Trp644=
XR_001744857.1:n.1940G=
XR_001744858.1:n.1823-3905G=
NM_001354609.2:c.1812G= NP_001341538.1:p.Trp604=
NM_001374244.1:c.1932G= NP_001361173.1:p.Trp644=
NM_001374258.1:c.1932G= MANE Plus Clinical NP_001361187.1:p.Trp644=
NM_004333.6:c.1812G= MANE Select NP_004324.2:p.Trp604=
NM_001378467.1:c.1821G= NP_001365396.1:p.Trp607=
NM_001378468.1:c.1812G= NP_001365397.1:p.Trp604=
NM_001378469.1:c.1746G= NP_001365398.1:p.Trp582=
NM_001378470.1:c.1710G= NP_001365399.1:p.Trp570=
NM_001378471.1:c.1701G= NP_001365400.1:p.Trp567=
NM_001378472.1:c.1656G= NP_001365401.1:p.Trp552=
NM_001378473.1:c.1656G= NP_001365402.1:p.Trp552=
NM_001378474.1:c.1812G= NP_001365403.1:p.Trp604=
NM_001378475.1:c.1548G= NP_001365404.1:p.Trp516=