Canonical Allele Identifier: CA1747732425

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140801283_140801287delinsTAAAA , CM000669.2:g.140801283_140801287delinsTAAAA	GRCh38
NC_000007.13:g.140501083_140501087delinsTAAAA , CM000669.1:g.140501083_140501087delinsTAAAA	GRCh37
NC_000007.12:g.140147552_140147556delinsTAAAA	NCBI36
NG_007873.3:g.128478_128482delinsTTTTA , LRG_299:g.128478_128482delinsTTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.860+125_860+129delinsTTTTA MANE Select	ENSP00000493543.1:n.860+125_860+129delinsTTTTA
ENST00000288602.11:c.860+125_860+129delinsTTTTA	ENSP00000288602.7:n.860+125_860+129delinsTTTTA
ENST00000496384.7:c.860+125_860+129delinsTTTTA	ENSP00000419060.2:n.860+125_860+129delinsTTTTA
ENST00000497784.2:c.*310+125_*310+129delinsTTTTA	ENSP00000420119.2:n.*310+125_*310+129delinsTTTTA
ENST00000642228.1:c.860+125_860+129delinsTTTTA	ENSP00000493678.1:n.860+125_860+129delinsTTTTA
ENST00000642272.1:n.892+125_892+129delinsTTTTA
ENST00000642875.1:n.354+125_354+129delinsTTTTA
ENST00000643356.1:n.586_590delinsTTTTA
ENST00000644120.1:n.1302+125_1302+129delinsTTTTA
ENST00000644905.1:n.949+125_949+129delinsTTTTA
ENST00000644969.2:c.860+125_860+129delinsTTTTA MANE Plus Clinical	ENSP00000496776.1:n.860+125_860+129delinsTTTTA
ENST00000646730.1:c.860+125_860+129delinsTTTTA	ENSP00000494784.1:n.860+125_860+129delinsTTTTA
ENST00000646891.1:c.860+125_860+129delinsTTTTA	ENSP00000493543.1:n.860+125_860+129delinsTTTTA
ENST00000288602.10:c.860+125_860+129delinsTTTTA	ENSP00000288602.6:n.860+125_860+129delinsTTTTA
ENST00000497784.1:c.895+125_895+129delinsTTTTA	ENSP00000420119.1:n.895+125_895+129delinsTTTTA
NM_004333.4:c.860+125_860+129delinsTTTTA , LRG_299t1:c.860+125_860+129delinsTTTTA	NP_004324.2:n.860+125_860+129delinsTTTTA
XM_005250045.1:c.860+125_860+129delinsTTTTA	XP_005250102.1:n.860+125_860+129delinsTTTTA
XM_005250046.1:c.860+125_860+129delinsTTTTA	XP_005250103.1:n.860+125_860+129delinsTTTTA
XM_011516529.1:c.860+125_860+129delinsTTTTA	XP_011514831.1:n.860+125_860+129delinsTTTTA
XM_011516530.1:c.860+125_860+129delinsTTTTA	XP_011514832.1:n.860+125_860+129delinsTTTTA
XR_242190.1:n.868+125_868+129delinsTTTTA
XR_927520.1:n.868+125_868+129delinsTTTTA
XR_927521.1:n.868+125_868+129delinsTTTTA
XR_927522.1:n.868+125_868+129delinsTTTTA
XR_927523.1:n.868+125_868+129delinsTTTTA
NM_001354609.1:c.860+125_860+129delinsTTTTA	NP_001341538.1:n.860+125_860+129delinsTTTTA
NM_004333.5:c.860+125_860+129delinsTTTTA	NP_004324.2:n.860+125_860+129delinsTTTTA
NR_148928.1:n.1165+125_1165+129delinsTTTTA
XM_017012558.1:c.860+125_860+129delinsTTTTA	XP_016868047.1:n.860+125_860+129delinsTTTTA
XM_017012559.1:c.860+125_860+129delinsTTTTA	XP_016868048.1:n.860+125_860+129delinsTTTTA
XR_001744857.1:n.868+125_868+129delinsTTTTA
XR_001744858.1:n.868+125_868+129delinsTTTTA
NM_001354609.2:c.860+125_860+129delinsTTTTA	NP_001341538.1:n.860+125_860+129delinsTTTTA
NM_001374244.1:c.860+125_860+129delinsTTTTA	NP_001361173.1:n.860+125_860+129delinsTTTTA
NM_001374258.1:c.860+125_860+129delinsTTTTA MANE Plus Clinical	NP_001361187.1:n.860+125_860+129delinsTTTTA
NM_004333.6:c.860+125_860+129delinsTTTTA MANE Select	NP_004324.2:n.860+125_860+129delinsTTTTA
NM_001378467.1:c.869+125_869+129delinsTTTTA	NP_001365396.1:n.869+125_869+129delinsTTTTA
NM_001378468.1:c.860+125_860+129delinsTTTTA	NP_001365397.1:n.860+125_860+129delinsTTTTA
NM_001378469.1:c.860+125_860+129delinsTTTTA	NP_001365398.1:n.860+125_860+129delinsTTTTA
NM_001378470.1:c.758+125_758+129delinsTTTTA	NP_001365399.1:n.758+125_758+129delinsTTTTA
NM_001378471.1:c.860+125_860+129delinsTTTTA	NP_001365400.1:n.860+125_860+129delinsTTTTA
NM_001378472.1:c.704+125_704+129delinsTTTTA	NP_001365401.1:n.704+125_704+129delinsTTTTA
NM_001378473.1:c.704+125_704+129delinsTTTTA	NP_001365402.1:n.704+125_704+129delinsTTTTA
NM_001378474.1:c.860+125_860+129delinsTTTTA	NP_001365403.1:n.860+125_860+129delinsTTTTA
NM_001378475.1:c.596+125_596+129delinsTTTTA	NP_001365404.1:n.596+125_596+129delinsTTTTA