Canonical Allele Identifier: CA458115476

Gene: BRAF

Linked Data

• dbSNP Id: rs1800386242
• MyVariant Identifiers: chr7:g.140476723T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140776923T>G , CM000669.2:g.140776923T>G	GRCh38
NC_000007.13:g.140476723T>G , CM000669.1:g.140476723T>G	GRCh37
NC_000007.12:g.140123192T>G	NCBI36
NG_007873.3:g.152842A>C , LRG_299:g.152842A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1683A>C MANE Select	ENSP00000493543.1:p.Ala561=
ENST00000288602.11:c.1803A>C	ENSP00000288602.7:p.Ala601=
ENST00000479537.6:c.353A>C
ENST00000496384.7:c.1683A>C	ENSP00000419060.2:p.Ala561=
ENST00000497784.2:c.*1133A>C	ENSP00000420119.2:n.*1133A>C
ENST00000642228.1:c.*761A>C	ENSP00000493678.1:n.*761A>C
ENST00000642875.1:n.1247A>C
ENST00000644120.1:n.2073A>C
ENST00000644650.1:c.779A>C
ENST00000644905.1:n.1772A>C
ENST00000644969.2:c.1803A>C MANE Plus Clinical	ENSP00000496776.1:p.Ala601=
ENST00000646730.1:c.1683A>C	ENSP00000494784.1:p.Ala561=
ENST00000646891.1:c.1683A>C	ENSP00000493543.1:p.Ala561=
ENST00000647434.1:c.726A>C	ENSP00000495132.1:p.Ala242=
ENST00000288602.10:c.1683A>C	ENSP00000288602.6:p.Ala561=
ENST00000496384.6:c.506A>C
ENST00000497784.1:c.1718A>C	ENSP00000420119.1:n.1718A>C
NM_004333.4:c.1683A>C , LRG_299t1:c.1683A>C	NP_004324.2:p.Ala561=
XM_005250045.1:c.1683A>C	XP_005250102.1:p.Ala561=
XM_005250046.1:c.1683A>C	XP_005250103.1:p.Ala561=
XM_011516529.1:c.1683A>C	XP_011514831.1:p.Ala561=
XM_011516530.1:c.1683A>C	XP_011514832.1:p.Ala561=
XR_242190.1:n.1691A>C
XR_927520.1:n.1691A>C
XR_927521.1:n.1691A>C
XR_927522.1:n.1691A>C
XR_927523.1:n.1691A>C
NM_001354609.1:c.1683A>C	NP_001341538.1:p.Ala561=
NM_004333.5:c.1683A>C	NP_004324.2:p.Ala561=
NR_148928.1:n.1988A>C
XM_017012558.1:c.1803A>C	XP_016868047.1:p.Ala601=
XM_017012559.1:c.1803A>C	XP_016868048.1:p.Ala601=
XR_001744857.1:n.1811A>C
XR_001744858.1:n.1811A>C
NM_001354609.2:c.1683A>C	NP_001341538.1:p.Ala561=
NM_001374244.1:c.1803A>C	NP_001361173.1:p.Ala601=
NM_001374258.1:c.1803A>C MANE Plus Clinical	NP_001361187.1:p.Ala601=
NM_004333.6:c.1683A>C MANE Select	NP_004324.2:p.Ala561=
NM_001378467.1:c.1692A>C	NP_001365396.1:p.Ala564=
NM_001378468.1:c.1683A>C	NP_001365397.1:p.Ala561=
NM_001378469.1:c.1617A>C	NP_001365398.1:p.Ala539=
NM_001378470.1:c.1581A>C	NP_001365399.1:p.Ala527=
NM_001378471.1:c.1572A>C	NP_001365400.1:p.Ala524=
NM_001378472.1:c.1527A>C	NP_001365401.1:p.Ala509=
NM_001378473.1:c.1527A>C	NP_001365402.1:p.Ala509=
NM_001378474.1:c.1683A>C	NP_001365403.1:p.Ala561=
NM_001378475.1:c.1419A>C	NP_001365404.1:p.Ala473=