Canonical Allele Identifier: CA369590472

Gene: BRAF

Linked Data

• dbSNP Id: rs1259806158
• gnomAD v2: 7-140500246-G-C
• gnomAD v4: 7-140800446-G-C
• MyVariant Identifiers: chr7:g.140500246G>C (hg19) ; chr7:g.140800446G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140800446G>C , CM000669.2:g.140800446G>C	GRCh38
NC_000007.13:g.140500246G>C , CM000669.1:g.140500246G>C	GRCh37
NC_000007.12:g.140146715G>C	NCBI36
NG_007873.3:g.129319C>G , LRG_299:g.129319C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.896C>G MANE Select	ENSP00000493543.1:p.Pro299Arg
ENST00000288602.11:c.896C>G	ENSP00000288602.7:p.Pro299Arg
ENST00000496384.7:c.896C>G	ENSP00000419060.2:p.Pro299Arg
ENST00000497784.2:c.*346C>G	ENSP00000420119.2:n.*346C>G
ENST00000642228.1:c.877C>G	ENSP00000493678.1:p.Gln293Glu
ENST00000642272.1:n.928C>G
ENST00000642875.1:n.390C>G
ENST00000644120.1:n.1338C>G
ENST00000644905.1:n.985C>G
ENST00000644969.2:c.896C>G MANE Plus Clinical	ENSP00000496776.1:p.Pro299Arg
ENST00000646730.1:c.896C>G	ENSP00000494784.1:p.Pro299Arg
ENST00000646891.1:c.896C>G	ENSP00000493543.1:p.Pro299Arg
ENST00000288602.10:c.896C>G	ENSP00000288602.6:p.Pro299Arg
ENST00000497784.1:c.931C>G	ENSP00000420119.1:n.931C>G
NM_004333.4:c.896C>G , LRG_299t1:c.896C>G	NP_004324.2:p.Pro299Arg
XM_005250045.1:c.896C>G	XP_005250102.1:p.Pro299Arg
XM_005250046.1:c.896C>G	XP_005250103.1:p.Pro299Arg
XM_011516529.1:c.896C>G	XP_011514831.1:p.Pro299Arg
XM_011516530.1:c.896C>G	XP_011514832.1:p.Pro299Arg
XR_242190.1:n.904C>G
XR_927520.1:n.904C>G
XR_927521.1:n.904C>G
XR_927522.1:n.904C>G
XR_927523.1:n.904C>G
NM_001354609.1:c.896C>G	NP_001341538.1:p.Pro299Arg
NM_004333.5:c.896C>G	NP_004324.2:p.Pro299Arg
NR_148928.1:n.1201C>G
XM_017012558.1:c.896C>G	XP_016868047.1:p.Pro299Arg
XM_017012559.1:c.896C>G	XP_016868048.1:p.Pro299Arg
XR_001744857.1:n.904C>G
XR_001744858.1:n.904C>G
NM_001354609.2:c.896C>G	NP_001341538.1:p.Pro299Arg
NM_001374244.1:c.896C>G	NP_001361173.1:p.Pro299Arg
NM_001374258.1:c.896C>G MANE Plus Clinical	NP_001361187.1:p.Pro299Arg
NM_004333.6:c.896C>G MANE Select	NP_004324.2:p.Pro299Arg
NM_001378467.1:c.905C>G	NP_001365396.1:p.Pro302Arg
NM_001378468.1:c.896C>G	NP_001365397.1:p.Pro299Arg
NM_001378469.1:c.896C>G	NP_001365398.1:p.Pro299Arg
NM_001378470.1:c.794C>G	NP_001365399.1:p.Pro265Arg
NM_001378471.1:c.896C>G	NP_001365400.1:p.Pro299Arg
NM_001378472.1:c.740C>G	NP_001365401.1:p.Pro247Arg
NM_001378473.1:c.740C>G	NP_001365402.1:p.Pro247Arg
NM_001378474.1:c.896C>G	NP_001365403.1:p.Pro299Arg
NM_001378475.1:c.632C>G	NP_001365404.1:p.Pro211Arg