Canonical Allele Identifier: CA458115647

Gene: BRAF

Linked Data

• ClinVar Variation Id: 2102994
• ClinVar RCV Id: RCV003019805
• dbSNP Id: rs1192815289
• MyVariant Identifiers: chr7:g.140476870A>G (hg19) ; chr7:g.140777070A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140777070A>G , CM000669.2:g.140777070A>G	GRCh38
NC_000007.13:g.140476870A>G , CM000669.1:g.140476870A>G	GRCh37
NC_000007.12:g.140123339A>G	NCBI36
NG_007873.3:g.152695T>C , LRG_299:g.152695T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1536T>C MANE Select	ENSP00000493543.1:p.Asn512=
ENST00000288602.11:c.1656T>C	ENSP00000288602.7:p.Asn552=
ENST00000479537.6:c.206T>C
ENST00000496384.7:c.1536T>C	ENSP00000419060.2:p.Asn512=
ENST00000497784.2:c.*986T>C	ENSP00000420119.2:n.*986T>C
ENST00000642228.1:c.*614T>C	ENSP00000493678.1:n.*614T>C
ENST00000642875.1:n.1100T>C
ENST00000644120.1:n.1926T>C
ENST00000644650.1:c.632T>C
ENST00000644905.1:n.1625T>C
ENST00000644969.2:c.1656T>C MANE Plus Clinical	ENSP00000496776.1:p.Asn552=
ENST00000646730.1:c.1536T>C	ENSP00000494784.1:p.Asn512=
ENST00000646891.1:c.1536T>C	ENSP00000493543.1:p.Asn512=
ENST00000647434.1:c.579T>C	ENSP00000495132.1:p.Asn193=
ENST00000288602.10:c.1536T>C	ENSP00000288602.6:p.Asn512=
ENST00000496384.6:c.359T>C
ENST00000497784.1:c.1571T>C	ENSP00000420119.1:n.1571T>C
NM_004333.4:c.1536T>C , LRG_299t1:c.1536T>C	NP_004324.2:p.Asn512=
XM_005250045.1:c.1536T>C	XP_005250102.1:p.Asn512=
XM_005250046.1:c.1536T>C	XP_005250103.1:p.Asn512=
XM_011516529.1:c.1536T>C	XP_011514831.1:p.Asn512=
XM_011516530.1:c.1536T>C	XP_011514832.1:p.Asn512=
XR_242190.1:n.1544T>C
XR_927520.1:n.1544T>C
XR_927521.1:n.1544T>C
XR_927522.1:n.1544T>C
XR_927523.1:n.1544T>C
NM_001354609.1:c.1536T>C	NP_001341538.1:p.Asn512=
NM_004333.5:c.1536T>C	NP_004324.2:p.Asn512=
NR_148928.1:n.1841T>C
XM_017012558.1:c.1656T>C	XP_016868047.1:p.Asn552=
XM_017012559.1:c.1656T>C	XP_016868048.1:p.Asn552=
XR_001744857.1:n.1664T>C
XR_001744858.1:n.1664T>C
NM_001354609.2:c.1536T>C	NP_001341538.1:p.Asn512=
NM_001374244.1:c.1656T>C	NP_001361173.1:p.Asn552=
NM_001374258.1:c.1656T>C MANE Plus Clinical	NP_001361187.1:p.Asn552=
NM_004333.6:c.1536T>C MANE Select	NP_004324.2:p.Asn512=
NM_001378467.1:c.1545T>C	NP_001365396.1:p.Asn515=
NM_001378468.1:c.1536T>C	NP_001365397.1:p.Asn512=
NM_001378469.1:c.1470T>C	NP_001365398.1:p.Asn490=
NM_001378470.1:c.1434T>C	NP_001365399.1:p.Asn478=
NM_001378471.1:c.1425T>C	NP_001365400.1:p.Asn475=
NM_001378472.1:c.1380T>C	NP_001365401.1:p.Asn460=
NM_001378473.1:c.1380T>C	NP_001365402.1:p.Asn460=
NM_001378474.1:c.1536T>C	NP_001365403.1:p.Asn512=
NM_001378475.1:c.1272T>C	NP_001365404.1:p.Asn424=