Canonical Allele Identifier: CA1747732332

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140801039_140801040delinsCG , CM000669.2:g.140801039_140801040delinsCG	GRCh38
NC_000007.13:g.140500839_140500840delinsCG , CM000669.1:g.140500839_140500840delinsCG	GRCh37
NC_000007.12:g.140147308_140147309delinsCG	NCBI36
NG_007873.3:g.128725_128726delinsCG , LRG_299:g.128725_128726delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.860+372_860+373delinsCG MANE Select	ENSP00000493543.1:n.860+372_860+373delinsCG
ENST00000288602.11:c.860+372_860+373delinsCG	ENSP00000288602.7:n.860+372_860+373delinsCG
ENST00000496384.7:c.860+372_860+373delinsCG	ENSP00000419060.2:n.860+372_860+373delinsCG
ENST00000497784.2:c.*310+372_*310+373delinsCG	ENSP00000420119.2:n.*310+372_*310+373delinsCG
ENST00000642228.1:c.860+372_860+373delinsCG	ENSP00000493678.1:n.860+372_860+373delinsCG
ENST00000642272.1:n.892+372_892+373delinsCG
ENST00000642875.1:n.354+372_354+373delinsCG
ENST00000643356.1:n.833_834delinsCG
ENST00000644120.1:n.1302+372_1302+373delinsCG
ENST00000644905.1:n.949+372_949+373delinsCG
ENST00000644969.2:c.860+372_860+373delinsCG MANE Plus Clinical	ENSP00000496776.1:n.860+372_860+373delinsCG
ENST00000646730.1:c.860+372_860+373delinsCG	ENSP00000494784.1:n.860+372_860+373delinsCG
ENST00000646891.1:c.860+372_860+373delinsCG	ENSP00000493543.1:n.860+372_860+373delinsCG
ENST00000288602.10:c.860+372_860+373delinsCG	ENSP00000288602.6:n.860+372_860+373delinsCG
ENST00000497784.1:c.895+372_895+373delinsCG	ENSP00000420119.1:n.895+372_895+373delinsCG
NM_004333.4:c.860+372_860+373delinsCG , LRG_299t1:c.860+372_860+373delinsCG	NP_004324.2:n.860+372_860+373delinsCG
XM_005250045.1:c.860+372_860+373delinsCG	XP_005250102.1:n.860+372_860+373delinsCG
XM_005250046.1:c.860+372_860+373delinsCG	XP_005250103.1:n.860+372_860+373delinsCG
XM_011516529.1:c.860+372_860+373delinsCG	XP_011514831.1:n.860+372_860+373delinsCG
XM_011516530.1:c.860+372_860+373delinsCG	XP_011514832.1:n.860+372_860+373delinsCG
XR_242190.1:n.868+372_868+373delinsCG
XR_927520.1:n.868+372_868+373delinsCG
XR_927521.1:n.868+372_868+373delinsCG
XR_927522.1:n.868+372_868+373delinsCG
XR_927523.1:n.868+372_868+373delinsCG
NM_001354609.1:c.860+372_860+373delinsCG	NP_001341538.1:n.860+372_860+373delinsCG
NM_004333.5:c.860+372_860+373delinsCG	NP_004324.2:n.860+372_860+373delinsCG
NR_148928.1:n.1165+372_1165+373delinsCG
XM_017012558.1:c.860+372_860+373delinsCG	XP_016868047.1:n.860+372_860+373delinsCG
XM_017012559.1:c.860+372_860+373delinsCG	XP_016868048.1:n.860+372_860+373delinsCG
XR_001744857.1:n.868+372_868+373delinsCG
XR_001744858.1:n.868+372_868+373delinsCG
NM_001354609.2:c.860+372_860+373delinsCG	NP_001341538.1:n.860+372_860+373delinsCG
NM_001374244.1:c.860+372_860+373delinsCG	NP_001361173.1:n.860+372_860+373delinsCG
NM_001374258.1:c.860+372_860+373delinsCG MANE Plus Clinical	NP_001361187.1:n.860+372_860+373delinsCG
NM_004333.6:c.860+372_860+373delinsCG MANE Select	NP_004324.2:n.860+372_860+373delinsCG
NM_001378467.1:c.869+372_869+373delinsCG	NP_001365396.1:n.869+372_869+373delinsCG
NM_001378468.1:c.860+372_860+373delinsCG	NP_001365397.1:n.860+372_860+373delinsCG
NM_001378469.1:c.860+372_860+373delinsCG	NP_001365398.1:n.860+372_860+373delinsCG
NM_001378470.1:c.758+372_758+373delinsCG	NP_001365399.1:n.758+372_758+373delinsCG
NM_001378471.1:c.860+372_860+373delinsCG	NP_001365400.1:n.860+372_860+373delinsCG
NM_001378472.1:c.704+372_704+373delinsCG	NP_001365401.1:n.704+372_704+373delinsCG
NM_001378473.1:c.704+372_704+373delinsCG	NP_001365402.1:n.704+372_704+373delinsCG
NM_001378474.1:c.860+372_860+373delinsCG	NP_001365403.1:n.860+372_860+373delinsCG
NM_001378475.1:c.596+372_596+373delinsCG	NP_001365404.1:n.596+372_596+373delinsCG