Canonical Allele Identifier: CA2685244381

Gene: BRAF

Linked Data

• gnomAD v4: 7-140801383-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140801383T>C , CM000669.2:g.140801383T>C	GRCh38
NC_000007.13:g.140501183T>C , CM000669.1:g.140501183T>C	GRCh37
NC_000007.12:g.140147652T>C	NCBI36
NG_007873.3:g.128382A>G , LRG_299:g.128382A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.860+29A>G MANE Select	ENSP00000493543.1:n.860+29A>G
ENST00000288602.11:c.860+29A>G	ENSP00000288602.7:n.860+29A>G
ENST00000496384.7:c.860+29A>G	ENSP00000419060.2:n.860+29A>G
ENST00000497784.2:c.*310+29A>G	ENSP00000420119.2:n.*310+29A>G
ENST00000642228.1:c.860+29A>G	ENSP00000493678.1:n.860+29A>G
ENST00000642272.1:n.892+29A>G
ENST00000642875.1:n.354+29A>G
ENST00000643356.1:n.490A>G
ENST00000644120.1:n.1302+29A>G
ENST00000644905.1:n.949+29A>G
ENST00000644969.2:c.860+29A>G MANE Plus Clinical	ENSP00000496776.1:n.860+29A>G
ENST00000646730.1:c.860+29A>G	ENSP00000494784.1:n.860+29A>G
ENST00000646891.1:c.860+29A>G	ENSP00000493543.1:n.860+29A>G
ENST00000288602.10:c.860+29A>G	ENSP00000288602.6:n.860+29A>G
ENST00000497784.1:c.895+29A>G	ENSP00000420119.1:n.895+29A>G
NM_004333.4:c.860+29A>G , LRG_299t1:c.860+29A>G	NP_004324.2:n.860+29A>G
XM_005250045.1:c.860+29A>G	XP_005250102.1:n.860+29A>G
XM_005250046.1:c.860+29A>G	XP_005250103.1:n.860+29A>G
XM_011516529.1:c.860+29A>G	XP_011514831.1:n.860+29A>G
XM_011516530.1:c.860+29A>G	XP_011514832.1:n.860+29A>G
XR_242190.1:n.868+29A>G
XR_927520.1:n.868+29A>G
XR_927521.1:n.868+29A>G
XR_927522.1:n.868+29A>G
XR_927523.1:n.868+29A>G
NM_001354609.1:c.860+29A>G	NP_001341538.1:n.860+29A>G
NM_004333.5:c.860+29A>G	NP_004324.2:n.860+29A>G
NR_148928.1:n.1165+29A>G
XM_017012558.1:c.860+29A>G	XP_016868047.1:n.860+29A>G
XM_017012559.1:c.860+29A>G	XP_016868048.1:n.860+29A>G
XR_001744857.1:n.868+29A>G
XR_001744858.1:n.868+29A>G
NM_001354609.2:c.860+29A>G	NP_001341538.1:n.860+29A>G
NM_001374244.1:c.860+29A>G	NP_001361173.1:n.860+29A>G
NM_001374258.1:c.860+29A>G MANE Plus Clinical	NP_001361187.1:n.860+29A>G
NM_004333.6:c.860+29A>G MANE Select	NP_004324.2:n.860+29A>G
NM_001378467.1:c.869+29A>G	NP_001365396.1:n.869+29A>G
NM_001378468.1:c.860+29A>G	NP_001365397.1:n.860+29A>G
NM_001378469.1:c.860+29A>G	NP_001365398.1:n.860+29A>G
NM_001378470.1:c.758+29A>G	NP_001365399.1:n.758+29A>G
NM_001378471.1:c.860+29A>G	NP_001365400.1:n.860+29A>G
NM_001378472.1:c.704+29A>G	NP_001365401.1:n.704+29A>G
NM_001378473.1:c.704+29A>G	NP_001365402.1:n.704+29A>G
NM_001378474.1:c.860+29A>G	NP_001365403.1:n.860+29A>G
NM_001378475.1:c.596+29A>G	NP_001365404.1:n.596+29A>G