Canonical Allele Identifier: CA457985905

Gene: BRAF

Linked Data

• MyVariant Identifiers: chr7:g.140449174A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140749374A>G , CM000669.2:g.140749374A>G	GRCh38
NC_000007.13:g.140449174A>G , CM000669.1:g.140449174A>G	GRCh37
NC_000007.12:g.140095643A>G	NCBI36
NG_007873.3:g.180391T>C , LRG_299:g.180391T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1905T>C MANE Select	ENSP00000493543.1:p.Phe635=
ENST00000288602.11:c.2025T>C	ENSP00000288602.7:p.Phe675=
ENST00000479537.6:c.575T>C
ENST00000496384.7:c.1905T>C	ENSP00000419060.2:p.Phe635=
ENST00000497784.2:c.*1355T>C	ENSP00000420119.2:n.*1355T>C
ENST00000642228.1:c.*983T>C	ENSP00000493678.1:n.*983T>C
ENST00000642875.1:n.1303T>C
ENST00000644120.1:n.2295T>C
ENST00000644650.1:c.1001T>C
ENST00000644905.1:n.2787T>C
ENST00000644969.2:c.2025T>C MANE Plus Clinical	ENSP00000496776.1:p.Phe675=
ENST00000646730.1:c.*481T>C	ENSP00000494784.1:n.*481T>C
ENST00000646891.1:c.1905T>C	ENSP00000493543.1:p.Phe635=
ENST00000647434.1:c.782T>C	ENSP00000495132.1:p.Phe261Ser
ENST00000288602.10:c.1905T>C	ENSP00000288602.6:p.Phe635=
ENST00000479537.5:c.189T>C	ENSP00000418033.1:p.Phe63=
ENST00000496384.6:c.728T>C
ENST00000497784.1:c.1940T>C	ENSP00000420119.1:n.1940T>C
NM_004333.4:c.1905T>C , LRG_299t1:c.1905T>C	NP_004324.2:p.Phe635=
XM_005250045.1:c.1905T>C	XP_005250102.1:p.Phe635=
XM_005250046.1:c.1905T>C	XP_005250103.1:p.Phe635=
XM_011516529.1:c.1905T>C	XP_011514831.1:p.Phe635=
XM_011516530.1:c.1739T>C	XP_011514832.1:p.Phe580Ser
XR_242190.1:n.1913T>C
XR_927520.1:n.1913T>C
XR_927521.1:n.1913T>C
XR_927522.1:n.1747T>C
XR_927523.1:n.1747T>C
NM_001354609.1:c.1905T>C	NP_001341538.1:p.Phe635=
NM_004333.5:c.1905T>C	NP_004324.2:p.Phe635=
NR_148928.1:n.3003T>C
XM_017012558.1:c.2025T>C	XP_016868047.1:p.Phe675=
XM_017012559.1:c.2025T>C	XP_016868048.1:p.Phe675=
XR_001744857.1:n.2033T>C
XR_001744858.1:n.1867T>C
NM_001354609.2:c.1905T>C	NP_001341538.1:p.Phe635=
NM_001374244.1:c.2025T>C	NP_001361173.1:p.Phe675=
NM_001374258.1:c.2025T>C MANE Plus Clinical	NP_001361187.1:p.Phe675=
NM_004333.6:c.1905T>C MANE Select	NP_004324.2:p.Phe635=
NM_001378467.1:c.1914T>C	NP_001365396.1:p.Phe638=
NM_001378468.1:c.1905T>C	NP_001365397.1:p.Phe635=
NM_001378469.1:c.1839T>C	NP_001365398.1:p.Phe613=
NM_001378470.1:c.1803T>C	NP_001365399.1:p.Phe601=
NM_001378471.1:c.1794T>C	NP_001365400.1:p.Phe598=
NM_001378472.1:c.1749T>C	NP_001365401.1:p.Phe583=
NM_001378473.1:c.1749T>C	NP_001365402.1:p.Phe583=
NM_001378474.1:c.1905T>C	NP_001365403.1:p.Phe635=
NM_001378475.1:c.1641T>C	NP_001365404.1:p.Phe547=