Canonical Allele Identifier: CA457985472

Gene: BRAF

Linked Data

• MyVariant Identifiers: chr7:g.140439738A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140739938A>G , CM000669.2:g.140739938A>G	GRCh38
NC_000007.13:g.140439738A>G , CM000669.1:g.140439738A>G	GRCh37
NC_000007.12:g.140086207A>G	NCBI36
NG_007873.3:g.189827T>C , LRG_299:g.189827T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.2001T>C MANE Select	ENSP00000493543.1:p.Phe667=
ENST00000288602.11:c.2121T>C	ENSP00000288602.7:p.Phe707=
ENST00000479537.6:c.753T>C
ENST00000496384.7:c.2001T>C	ENSP00000419060.2:p.Phe667=
ENST00000497784.2:c.*1451T>C	ENSP00000420119.2:n.*1451T>C
ENST00000642228.1:c.*1079T>C	ENSP00000493678.1:n.*1079T>C
ENST00000642875.1:n.1399T>C
ENST00000644120.1:n.2391T>C
ENST00000644650.1:c.1300T>C
ENST00000644905.1:n.2883T>C
ENST00000644969.2:c.2121T>C MANE Plus Clinical	ENSP00000496776.1:p.Phe707=
ENST00000645443.1:n.1780T>C
ENST00000646730.1:c.*659T>C	ENSP00000494784.1:n.*659T>C
ENST00000646891.1:c.2001T>C	ENSP00000493543.1:p.Phe667=
ENST00000647434.1:c.878T>C	ENSP00000495132.1:n.878T>C
ENST00000288602.10:c.2001T>C	ENSP00000288602.6:p.Phe667=
ENST00000479537.5:c.367T>C	ENSP00000418033.1:n.367T>C
ENST00000496384.6:c.824T>C
ENST00000497784.1:c.2036T>C	ENSP00000420119.1:n.2036T>C
NM_004333.4:c.2001T>C , LRG_299t1:c.2001T>C	NP_004324.2:p.Phe667=
XM_005250045.1:c.2001T>C	XP_005250102.1:p.Phe667=
XM_005250046.1:c.2001T>C	XP_005250103.1:p.Phe667=
XM_011516529.1:c.2001T>C	XP_011514831.1:p.Phe667=
XR_242190.1:n.2091T>C
XR_927520.1:n.2130T>C
XR_927521.1:n.2212T>C
XR_927522.1:n.1843T>C
XR_927523.1:n.1925T>C
NM_001354609.1:c.2001T>C	NP_001341538.1:p.Phe667=
NM_004333.5:c.2001T>C	NP_004324.2:p.Phe667=
NR_148928.1:n.3099T>C
XM_017012558.1:c.2121T>C	XP_016868047.1:p.Phe707=
XM_017012559.1:c.2121T>C	XP_016868048.1:p.Phe707=
XR_001744857.1:n.2211T>C
XR_001744858.1:n.1963T>C
NM_001354609.2:c.2001T>C	NP_001341538.1:p.Phe667=
NM_001374244.1:c.2121T>C	NP_001361173.1:p.Phe707=
NM_001374258.1:c.2121T>C MANE Plus Clinical	NP_001361187.1:p.Phe707=
NM_004333.6:c.2001T>C MANE Select	NP_004324.2:p.Phe667=
NM_001378467.1:c.2010T>C	NP_001365396.1:p.Phe670=
NM_001378468.1:c.2001T>C	NP_001365397.1:p.Phe667=
NM_001378469.1:c.1935T>C	NP_001365398.1:p.Phe645=
NM_001378470.1:c.1899T>C	NP_001365399.1:p.Phe633=
NM_001378471.1:c.1890T>C	NP_001365400.1:p.Phe630=
NM_001378472.1:c.1845T>C	NP_001365401.1:p.Phe615=
NM_001378473.1:c.1845T>C	NP_001365402.1:p.Phe615=
NM_001378474.1:c.2001T>C	NP_001365403.1:p.Phe667=
NM_001378475.1:c.1737T>C	NP_001365404.1:p.Phe579=