Canonical Allele Identifier: CA457985470

Gene: BRAF

Linked Data

• MyVariant Identifiers: chr7:g.140439732C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140739932C>G , CM000669.2:g.140739932C>G	GRCh38
NC_000007.13:g.140439732C>G , CM000669.1:g.140439732C>G	GRCh37
NC_000007.12:g.140086201C>G	NCBI36
NG_007873.3:g.189833G>C , LRG_299:g.189833G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.2007G>C MANE Select	ENSP00000493543.1:p.Val669=
ENST00000288602.11:c.2127G>C	ENSP00000288602.7:p.Val709=
ENST00000479537.6:c.759G>C
ENST00000496384.7:c.2007G>C	ENSP00000419060.2:p.Val669=
ENST00000497784.2:c.*1457G>C	ENSP00000420119.2:n.*1457G>C
ENST00000642228.1:c.*1085G>C	ENSP00000493678.1:n.*1085G>C
ENST00000642875.1:n.1405G>C
ENST00000644120.1:n.2397G>C
ENST00000644650.1:c.1306G>C
ENST00000644905.1:n.2889G>C
ENST00000644969.2:c.2127G>C MANE Plus Clinical	ENSP00000496776.1:p.Val709=
ENST00000645443.1:n.1786G>C
ENST00000646730.1:c.*665G>C	ENSP00000494784.1:n.*665G>C
ENST00000646891.1:c.2007G>C	ENSP00000493543.1:p.Val669=
ENST00000647434.1:c.884G>C	ENSP00000495132.1:n.884G>C
ENST00000288602.10:c.2007G>C	ENSP00000288602.6:p.Val669=
ENST00000479537.5:c.373G>C	ENSP00000418033.1:n.373G>C
ENST00000496384.6:c.830G>C
ENST00000497784.1:c.2042G>C	ENSP00000420119.1:n.2042G>C
NM_004333.4:c.2007G>C , LRG_299t1:c.2007G>C	NP_004324.2:p.Val669=
XM_005250045.1:c.2007G>C	XP_005250102.1:p.Val669=
XM_005250046.1:c.2007G>C	XP_005250103.1:p.Val669=
XM_011516529.1:c.2007G>C	XP_011514831.1:p.Val669=
XR_242190.1:n.2097G>C
XR_927520.1:n.2136G>C
XR_927521.1:n.2218G>C
XR_927522.1:n.1849G>C
XR_927523.1:n.1931G>C
NM_001354609.1:c.2007G>C	NP_001341538.1:p.Val669=
NM_004333.5:c.2007G>C	NP_004324.2:p.Val669=
NR_148928.1:n.3105G>C
XM_017012558.1:c.2127G>C	XP_016868047.1:p.Val709=
XM_017012559.1:c.2127G>C	XP_016868048.1:p.Val709=
XR_001744857.1:n.2217G>C
XR_001744858.1:n.1969G>C
NM_001354609.2:c.2007G>C	NP_001341538.1:p.Val669=
NM_001374244.1:c.2127G>C	NP_001361173.1:p.Val709=
NM_001374258.1:c.2127G>C MANE Plus Clinical	NP_001361187.1:p.Val709=
NM_004333.6:c.2007G>C MANE Select	NP_004324.2:p.Val669=
NM_001378467.1:c.2016G>C	NP_001365396.1:p.Val672=
NM_001378468.1:c.2007G>C	NP_001365397.1:p.Val669=
NM_001378469.1:c.1941G>C	NP_001365398.1:p.Val647=
NM_001378470.1:c.1905G>C	NP_001365399.1:p.Val635=
NM_001378471.1:c.1896G>C	NP_001365400.1:p.Val632=
NM_001378472.1:c.1851G>C	NP_001365401.1:p.Val617=
NM_001378473.1:c.1851G>C	NP_001365402.1:p.Val617=
NM_001378474.1:c.2007G>C	NP_001365403.1:p.Val669=
NM_001378475.1:c.1743G>C	NP_001365404.1:p.Val581=