Canonical Allele Identifier: CA1747726008
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140777076A= , CM000669.2:g.140777076A= GRCh38
NC_000007.13:g.140476876A= , CM000669.1:g.140476876A= GRCh37
NC_000007.12:g.140123345A= NCBI36
NG_007873.3:g.152689T= , LRG_299:g.152689T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1530T= MANE Select ENSP00000493543.1:p.His510=
ENST00000288602.11:c.1650T= ENSP00000288602.7:p.His550=
ENST00000479537.6:c.200T=
ENST00000496384.7:c.1530T= ENSP00000419060.2:p.His510=
ENST00000497784.2:c.*980T= ENSP00000420119.2:n.*980T=
ENST00000642228.1:c.*608T= ENSP00000493678.1:n.*608T=
ENST00000642875.1:n.1094T=
ENST00000644120.1:n.1920T=
ENST00000644650.1:c.626T=
ENST00000644905.1:n.1619T=
ENST00000644969.2:c.1650T= MANE Plus Clinical ENSP00000496776.1:p.His550=
ENST00000646730.1:c.1530T= ENSP00000494784.1:p.His510=
ENST00000646891.1:c.1530T= ENSP00000493543.1:p.His510=
ENST00000647434.1:c.573T= ENSP00000495132.1:p.His191=
ENST00000288602.10:c.1530T= ENSP00000288602.6:p.His510=
ENST00000496384.6:c.353T=
ENST00000497784.1:c.1565T= ENSP00000420119.1:n.1565T=
NM_004333.4:c.1530T= , LRG_299t1:c.1530T= NP_004324.2:p.His510=
XM_005250045.1:c.1530T= XP_005250102.1:p.His510=
XM_005250046.1:c.1530T= XP_005250103.1:p.His510=
XM_011516529.1:c.1530T= XP_011514831.1:p.His510=
XM_011516530.1:c.1530T= XP_011514832.1:p.His510=
XR_242190.1:n.1538T=
XR_927520.1:n.1538T=
XR_927521.1:n.1538T=
XR_927522.1:n.1538T=
XR_927523.1:n.1538T=
NM_001354609.1:c.1530T= NP_001341538.1:p.His510=
NM_004333.5:c.1530T= NP_004324.2:p.His510=
NR_148928.1:n.1835T=
XM_017012558.1:c.1650T= XP_016868047.1:p.His550=
XM_017012559.1:c.1650T= XP_016868048.1:p.His550=
XR_001744857.1:n.1658T=
XR_001744858.1:n.1658T=
NM_001354609.2:c.1530T= NP_001341538.1:p.His510=
NM_001374244.1:c.1650T= NP_001361173.1:p.His550=
NM_001374258.1:c.1650T= MANE Plus Clinical NP_001361187.1:p.His550=
NM_004333.6:c.1530T= MANE Select NP_004324.2:p.His510=
NM_001378467.1:c.1539T= NP_001365396.1:p.His513=
NM_001378468.1:c.1530T= NP_001365397.1:p.His510=
NM_001378469.1:c.1464T= NP_001365398.1:p.His488=
NM_001378470.1:c.1428T= NP_001365399.1:p.His476=
NM_001378471.1:c.1419T= NP_001365400.1:p.His473=
NM_001378472.1:c.1374T= NP_001365401.1:p.His458=
NM_001378473.1:c.1374T= NP_001365402.1:p.His458=
NM_001378474.1:c.1530T= NP_001365403.1:p.His510=
NM_001378475.1:c.1266T= NP_001365404.1:p.His422=