Canonical Allele Identifier: CA1747715153
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140778126A= , CM000669.2:g.140778126A= GRCh38
NC_000007.13:g.140477926A= , CM000669.1:g.140477926A= GRCh37
NC_000007.12:g.140124395A= NCBI36
NG_007873.3:g.151639T= , LRG_299:g.151639T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1433-51T= MANE Select ENSP00000493543.1:n.1433-51T=
ENST00000288602.11:c.1553-51T= ENSP00000288602.7:n.1553-51T=
ENST00000479537.6:c.103-51T=
ENST00000496384.7:c.1433-51T= ENSP00000419060.2:n.1433-51T=
ENST00000497784.2:c.*883-51T= ENSP00000420119.2:n.*883-51T=
ENST00000642228.1:c.*511-51T= ENSP00000493678.1:n.*511-51T=
ENST00000642875.1:n.997-51T=
ENST00000644120.1:n.1823-51T=
ENST00000644650.1:c.529-51T=
ENST00000644905.1:n.1522-51T=
ENST00000644969.2:c.1553-51T= MANE Plus Clinical ENSP00000496776.1:n.1553-51T=
ENST00000646730.1:c.1433-51T= ENSP00000494784.1:n.1433-51T=
ENST00000646891.1:c.1433-51T= ENSP00000493543.1:n.1433-51T=
ENST00000647434.1:c.476-51T= ENSP00000495132.1:n.476-51T=
ENST00000288602.10:c.1433-51T= ENSP00000288602.6:n.1433-51T=
ENST00000496384.6:c.256-51T=
ENST00000497784.1:c.1468-51T= ENSP00000420119.1:n.1468-51T=
NM_004333.4:c.1433-51T= , LRG_299t1:c.1433-51T= NP_004324.2:n.1433-51T=
XM_005250045.1:c.1433-51T= XP_005250102.1:n.1433-51T=
XM_005250046.1:c.1433-51T= XP_005250103.1:n.1433-51T=
XM_011516529.1:c.1433-51T= XP_011514831.1:n.1433-51T=
XM_011516530.1:c.1433-51T= XP_011514832.1:n.1433-51T=
XR_242190.1:n.1441-51T=
XR_927520.1:n.1441-51T=
XR_927521.1:n.1441-51T=
XR_927522.1:n.1441-51T=
XR_927523.1:n.1441-51T=
NM_001354609.1:c.1433-51T= NP_001341538.1:n.1433-51T=
NM_004333.5:c.1433-51T= NP_004324.2:n.1433-51T=
NR_148928.1:n.1738-51T=
XM_017012558.1:c.1553-51T= XP_016868047.1:n.1553-51T=
XM_017012559.1:c.1553-51T= XP_016868048.1:n.1553-51T=
XR_001744857.1:n.1561-51T=
XR_001744858.1:n.1561-51T=
NM_001354609.2:c.1433-51T= NP_001341538.1:n.1433-51T=
NM_001374244.1:c.1553-51T= NP_001361173.1:n.1553-51T=
NM_001374258.1:c.1553-51T= MANE Plus Clinical NP_001361187.1:n.1553-51T=
NM_004333.6:c.1433-51T= MANE Select NP_004324.2:n.1433-51T=
NM_001378467.1:c.1442-51T= NP_001365396.1:n.1442-51T=
NM_001378468.1:c.1433-51T= NP_001365397.1:n.1433-51T=
NM_001378469.1:c.1367-51T= NP_001365398.1:n.1367-51T=
NM_001378470.1:c.1331-51T= NP_001365399.1:n.1331-51T=
NM_001378471.1:c.1322-51T= NP_001365400.1:n.1322-51T=
NM_001378472.1:c.1277-51T= NP_001365401.1:n.1277-51T=
NM_001378473.1:c.1277-51T= NP_001365402.1:n.1277-51T=
NM_001378474.1:c.1433-51T= NP_001365403.1:n.1433-51T=
NM_001378475.1:c.1169-51T= NP_001365404.1:n.1169-51T=