Canonical Allele Identifier: CA369543300

Gene: BRAF

Linked Data

• dbSNP Id: rs121913340
• MyVariant Identifiers: chr7:g.140453179C>A (hg19) ; chr7:g.140753379C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753379C>A , CM000669.2:g.140753379C>A	GRCh38
NC_000007.13:g.140453179C>A , CM000669.1:g.140453179C>A	GRCh37
NC_000007.12:g.140099648C>A	NCBI36
NG_007873.3:g.176386G>T , LRG_299:g.176386G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1756G>T MANE Select	ENSP00000493543.1:p.Glu586Ter
ENST00000288602.11:c.1876G>T	ENSP00000288602.7:p.Glu626Ter
ENST00000479537.6:c.426G>T
ENST00000496384.7:c.1756G>T	ENSP00000419060.2:p.Glu586Ter
ENST00000497784.2:c.*1206G>T	ENSP00000420119.2:n.*1206G>T
ENST00000642228.1:c.*834G>T	ENSP00000493678.1:n.*834G>T
ENST00000642875.1:n.1259-3961G>T
ENST00000644120.1:n.2146G>T
ENST00000644650.1:c.852G>T
ENST00000644905.1:n.2638G>T
ENST00000644969.2:c.1876G>T MANE Plus Clinical	ENSP00000496776.1:p.Glu626Ter
ENST00000646730.1:c.*332G>T	ENSP00000494784.1:n.*332G>T
ENST00000646891.1:c.1756G>T	ENSP00000493543.1:p.Glu586Ter
ENST00000647434.1:c.738-3961G>T	ENSP00000495132.1:n.738-3961G>T
ENST00000288602.10:c.1756G>T	ENSP00000288602.6:p.Glu586Ter
ENST00000479537.5:c.40G>T	ENSP00000418033.1:p.Glu14Ter
ENST00000496384.6:c.579G>T
ENST00000497784.1:c.1791G>T	ENSP00000420119.1:n.1791G>T
NM_004333.4:c.1756G>T , LRG_299t1:c.1756G>T	NP_004324.2:p.Glu586Ter
XM_005250045.1:c.1756G>T	XP_005250102.1:p.Glu586Ter
XM_005250046.1:c.1756G>T	XP_005250103.1:p.Glu586Ter
XM_011516529.1:c.1756G>T	XP_011514831.1:p.Glu586Ter
XM_011516530.1:c.1695-3961G>T	XP_011514832.1:n.1695-3961G>T
XR_242190.1:n.1764G>T
XR_927520.1:n.1764G>T
XR_927521.1:n.1764G>T
XR_927522.1:n.1703-3961G>T
XR_927523.1:n.1703-3961G>T
NM_001354609.1:c.1756G>T	NP_001341538.1:p.Glu586Ter
NM_004333.5:c.1756G>T	NP_004324.2:p.Glu586Ter
NR_148928.1:n.2854G>T
XM_017012558.1:c.1876G>T	XP_016868047.1:p.Glu626Ter
XM_017012559.1:c.1876G>T	XP_016868048.1:p.Glu626Ter
XR_001744857.1:n.1884G>T
XR_001744858.1:n.1823-3961G>T
NM_001354609.2:c.1756G>T	NP_001341538.1:p.Glu586Ter
NM_001374244.1:c.1876G>T	NP_001361173.1:p.Glu626Ter
NM_001374258.1:c.1876G>T MANE Plus Clinical	NP_001361187.1:p.Glu626Ter
NM_004333.6:c.1756G>T MANE Select	NP_004324.2:p.Glu586Ter
NM_001378467.1:c.1765G>T	NP_001365396.1:p.Glu589Ter
NM_001378468.1:c.1756G>T	NP_001365397.1:p.Glu586Ter
NM_001378469.1:c.1690G>T	NP_001365398.1:p.Glu564Ter
NM_001378470.1:c.1654G>T	NP_001365399.1:p.Glu552Ter
NM_001378471.1:c.1645G>T	NP_001365400.1:p.Glu549Ter
NM_001378472.1:c.1600G>T	NP_001365401.1:p.Glu534Ter
NM_001378473.1:c.1600G>T	NP_001365402.1:p.Glu534Ter
NM_001378474.1:c.1756G>T	NP_001365403.1:p.Glu586Ter
NM_001378475.1:c.1492G>T	NP_001365404.1:p.Glu498Ter