Canonical Allele Identifier: CA458115954

Gene: BRAF

Linked Data

• dbSNP Id: rs750556299
• MyVariant Identifiers: chr7:g.140481443C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140781643C>G , CM000669.2:g.140781643C>G	GRCh38
NC_000007.13:g.140481443C>G , CM000669.1:g.140481443C>G	GRCh37
NC_000007.12:g.140127912C>G	NCBI36
NG_007873.3:g.148122G>C , LRG_299:g.148122G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1365G>C MANE Select	ENSP00000493543.1:p.Gly455=
ENST00000288602.11:c.1485G>C	ENSP00000288602.7:p.Gly495=
ENST00000479537.6:c.35G>C
ENST00000496384.7:c.1365G>C	ENSP00000419060.2:p.Gly455=
ENST00000497784.2:c.*815G>C	ENSP00000420119.2:n.*815G>C
ENST00000642228.1:c.*443G>C	ENSP00000493678.1:n.*443G>C
ENST00000642875.1:n.807G>C
ENST00000644120.1:n.1755G>C
ENST00000644650.1:c.461G>C
ENST00000644905.1:n.1454G>C
ENST00000644969.2:c.1485G>C MANE Plus Clinical	ENSP00000496776.1:p.Gly495=
ENST00000646334.1:n.495G>C
ENST00000646730.1:c.1365G>C	ENSP00000494784.1:p.Gly455=
ENST00000646891.1:c.1365G>C	ENSP00000493543.1:p.Gly455=
ENST00000647434.1:c.408G>C	ENSP00000495132.1:p.Gly136=
ENST00000288602.10:c.1365G>C	ENSP00000288602.6:p.Gly455=
ENST00000496384.6:c.188G>C
ENST00000497784.1:c.1400G>C	ENSP00000420119.1:n.1400G>C
NM_004333.4:c.1365G>C , LRG_299t1:c.1365G>C	NP_004324.2:p.Gly455=
XM_005250045.1:c.1365G>C	XP_005250102.1:p.Gly455=
XM_005250046.1:c.1365G>C	XP_005250103.1:p.Gly455=
XM_011516529.1:c.1365G>C	XP_011514831.1:p.Gly455=
XM_011516530.1:c.1365G>C	XP_011514832.1:p.Gly455=
XR_242190.1:n.1373G>C
XR_927520.1:n.1373G>C
XR_927521.1:n.1373G>C
XR_927522.1:n.1373G>C
XR_927523.1:n.1373G>C
NM_001354609.1:c.1365G>C	NP_001341538.1:p.Gly455=
NM_004333.5:c.1365G>C	NP_004324.2:p.Gly455=
NR_148928.1:n.1670G>C
XM_017012558.1:c.1485G>C	XP_016868047.1:p.Gly495=
XM_017012559.1:c.1485G>C	XP_016868048.1:p.Gly495=
XR_001744857.1:n.1493G>C
XR_001744858.1:n.1493G>C
NM_001354609.2:c.1365G>C	NP_001341538.1:p.Gly455=
NM_001374244.1:c.1485G>C	NP_001361173.1:p.Gly495=
NM_001374258.1:c.1485G>C MANE Plus Clinical	NP_001361187.1:p.Gly495=
NM_004333.6:c.1365G>C MANE Select	NP_004324.2:p.Gly455=
NM_001378467.1:c.1374G>C	NP_001365396.1:p.Gly458=
NM_001378468.1:c.1365G>C	NP_001365397.1:p.Gly455=
NM_001378469.1:c.1299G>C	NP_001365398.1:p.Gly433=
NM_001378470.1:c.1263G>C	NP_001365399.1:p.Gly421=
NM_001378471.1:c.1254G>C	NP_001365400.1:p.Gly418=
NM_001378472.1:c.1209G>C	NP_001365401.1:p.Gly403=
NM_001378473.1:c.1209G>C	NP_001365402.1:p.Gly403=
NM_001378474.1:c.1365G>C	NP_001365403.1:p.Gly455=
NM_001378475.1:c.1101G>C	NP_001365404.1:p.Gly367=