Canonical Allele Identifier: CA457985880

Gene: BRAF

Linked Data

• MyVariant Identifiers: chr7:g.140449168T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140749368T>G , CM000669.2:g.140749368T>G	GRCh38
NC_000007.13:g.140449168T>G , CM000669.1:g.140449168T>G	GRCh37
NC_000007.12:g.140095637T>G	NCBI36
NG_007873.3:g.180397A>C , LRG_299:g.180397A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1911A>C MANE Select	ENSP00000493543.1:p.Ser637=
ENST00000288602.11:c.2031A>C	ENSP00000288602.7:p.Ser677=
ENST00000479537.6:c.581A>C
ENST00000496384.7:c.1911A>C	ENSP00000419060.2:p.Ser637=
ENST00000497784.2:c.*1361A>C	ENSP00000420119.2:n.*1361A>C
ENST00000642228.1:c.*989A>C	ENSP00000493678.1:n.*989A>C
ENST00000642875.1:n.1309A>C
ENST00000644120.1:n.2301A>C
ENST00000644650.1:c.1007A>C
ENST00000644905.1:n.2793A>C
ENST00000644969.2:c.2031A>C MANE Plus Clinical	ENSP00000496776.1:p.Ser677=
ENST00000646730.1:c.*487A>C	ENSP00000494784.1:n.*487A>C
ENST00000646891.1:c.1911A>C	ENSP00000493543.1:p.Ser637=
ENST00000647434.1:c.788A>C	ENSP00000495132.1:p.Gln263Pro
ENST00000288602.10:c.1911A>C	ENSP00000288602.6:p.Ser637=
ENST00000479537.5:c.195A>C	ENSP00000418033.1:p.Ser65=
ENST00000496384.6:c.734A>C
ENST00000497784.1:c.1946A>C	ENSP00000420119.1:n.1946A>C
NM_004333.4:c.1911A>C , LRG_299t1:c.1911A>C	NP_004324.2:p.Ser637=
XM_005250045.1:c.1911A>C	XP_005250102.1:p.Ser637=
XM_005250046.1:c.1911A>C	XP_005250103.1:p.Ser637=
XM_011516529.1:c.1911A>C	XP_011514831.1:p.Ser637=
XM_011516530.1:c.1745A>C	XP_011514832.1:p.Gln582Pro
XR_242190.1:n.1919A>C
XR_927520.1:n.1919A>C
XR_927521.1:n.1919A>C
XR_927522.1:n.1753A>C
XR_927523.1:n.1753A>C
NM_001354609.1:c.1911A>C	NP_001341538.1:p.Ser637=
NM_004333.5:c.1911A>C	NP_004324.2:p.Ser637=
NR_148928.1:n.3009A>C
XM_017012558.1:c.2031A>C	XP_016868047.1:p.Ser677=
XM_017012559.1:c.2031A>C	XP_016868048.1:p.Ser677=
XR_001744857.1:n.2039A>C
XR_001744858.1:n.1873A>C
NM_001354609.2:c.1911A>C	NP_001341538.1:p.Ser637=
NM_001374244.1:c.2031A>C	NP_001361173.1:p.Ser677=
NM_001374258.1:c.2031A>C MANE Plus Clinical	NP_001361187.1:p.Ser677=
NM_004333.6:c.1911A>C MANE Select	NP_004324.2:p.Ser637=
NM_001378467.1:c.1920A>C	NP_001365396.1:p.Ser640=
NM_001378468.1:c.1911A>C	NP_001365397.1:p.Ser637=
NM_001378469.1:c.1845A>C	NP_001365398.1:p.Ser615=
NM_001378470.1:c.1809A>C	NP_001365399.1:p.Ser603=
NM_001378471.1:c.1800A>C	NP_001365400.1:p.Ser600=
NM_001378472.1:c.1755A>C	NP_001365401.1:p.Ser585=
NM_001378473.1:c.1755A>C	NP_001365402.1:p.Ser585=
NM_001378474.1:c.1911A>C	NP_001365403.1:p.Ser637=
NM_001378475.1:c.1647A>C	NP_001365404.1:p.Ser549=