Canonical Allele Identifier: CA1747718314
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781615A= , CM000669.2:g.140781615A= GRCh38
NC_000007.13:g.140481415A= , CM000669.1:g.140481415A= GRCh37
NC_000007.12:g.140127884A= NCBI36
NG_007873.3:g.148150T= , LRG_299:g.148150T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1393T= MANE Select ENSP00000493543.1:p.Ser465=
ENST00000288602.11:c.1513T= ENSP00000288602.7:p.Ser505=
ENST00000479537.6:c.63T=
ENST00000496384.7:c.1393T= ENSP00000419060.2:p.Ser465=
ENST00000497784.2:c.*843T= ENSP00000420119.2:n.*843T=
ENST00000642228.1:c.*471T= ENSP00000493678.1:n.*471T=
ENST00000642875.1:n.835T=
ENST00000644120.1:n.1783T=
ENST00000644650.1:c.489T=
ENST00000644905.1:n.1482T=
ENST00000644969.2:c.1513T= MANE Plus Clinical ENSP00000496776.1:p.Ser505=
ENST00000646334.1:n.523T=
ENST00000646730.1:c.1393T= ENSP00000494784.1:p.Ser465=
ENST00000646891.1:c.1393T= ENSP00000493543.1:p.Ser465=
ENST00000647434.1:c.436T= ENSP00000495132.1:p.Ser146=
ENST00000288602.10:c.1393T= ENSP00000288602.6:p.Ser465=
ENST00000496384.6:c.216T=
ENST00000497784.1:c.1428T= ENSP00000420119.1:n.1428T=
NM_004333.4:c.1393T= , LRG_299t1:c.1393T= NP_004324.2:p.Ser465=
XM_005250045.1:c.1393T= XP_005250102.1:p.Ser465=
XM_005250046.1:c.1393T= XP_005250103.1:p.Ser465=
XM_011516529.1:c.1393T= XP_011514831.1:p.Ser465=
XM_011516530.1:c.1393T= XP_011514832.1:p.Ser465=
XR_242190.1:n.1401T=
XR_927520.1:n.1401T=
XR_927521.1:n.1401T=
XR_927522.1:n.1401T=
XR_927523.1:n.1401T=
NM_001354609.1:c.1393T= NP_001341538.1:p.Ser465=
NM_004333.5:c.1393T= NP_004324.2:p.Ser465=
NR_148928.1:n.1698T=
XM_017012558.1:c.1513T= XP_016868047.1:p.Ser505=
XM_017012559.1:c.1513T= XP_016868048.1:p.Ser505=
XR_001744857.1:n.1521T=
XR_001744858.1:n.1521T=
NM_001354609.2:c.1393T= NP_001341538.1:p.Ser465=
NM_001374244.1:c.1513T= NP_001361173.1:p.Ser505=
NM_001374258.1:c.1513T= MANE Plus Clinical NP_001361187.1:p.Ser505=
NM_004333.6:c.1393T= MANE Select NP_004324.2:p.Ser465=
NM_001378467.1:c.1402T= NP_001365396.1:p.Ser468=
NM_001378468.1:c.1393T= NP_001365397.1:p.Ser465=
NM_001378469.1:c.1327T= NP_001365398.1:p.Ser443=
NM_001378470.1:c.1291T= NP_001365399.1:p.Ser431=
NM_001378471.1:c.1282T= NP_001365400.1:p.Ser428=
NM_001378472.1:c.1237T= NP_001365401.1:p.Ser413=
NM_001378473.1:c.1237T= NP_001365402.1:p.Ser413=
NM_001378474.1:c.1393T= NP_001365403.1:p.Ser465=
NM_001378475.1:c.1129T= NP_001365404.1:p.Ser377=