Canonical Allele Identifier: CA215454

Gene: BRAF

Linked Data

• ClinVar Variation Id: 41446
• ClinVar RCV Id: RCV000034332 ; RCV000150201
• dbSNP Id: rs121913364
• MyVariant Identifiers: chr7:g.140453134T>G (hg19) ; chr7:g.140753334T>G (hg38)
• PubMed: PMID:16953233 ; PMID:19206169 ; PMID:26619011

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753334T>G , CM000669.2:g.140753334T>G	GRCh38
NC_000007.13:g.140453134T>G , CM000669.1:g.140453134T>G	GRCh37
NC_000007.12:g.140099603T>G	NCBI36
NG_007873.3:g.176431A>C , LRG_299:g.176431A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1801A>C MANE Select	ENSP00000493543.1:p.Lys601Gln
ENST00000288602.11:c.1921A>C	ENSP00000288602.7:p.Lys641Gln
ENST00000479537.6:c.471A>C
ENST00000496384.7:c.1801A>C	ENSP00000419060.2:p.Lys601Gln
ENST00000497784.2:c.*1251A>C	ENSP00000420119.2:n.*1251A>C
ENST00000642228.1:c.*879A>C	ENSP00000493678.1:n.*879A>C
ENST00000642875.1:n.1259-3916A>C
ENST00000644120.1:n.2191A>C
ENST00000644650.1:c.897A>C
ENST00000644905.1:n.2683A>C
ENST00000644969.2:c.1921A>C MANE Plus Clinical	ENSP00000496776.1:p.Lys641Gln
ENST00000646730.1:c.*377A>C	ENSP00000494784.1:n.*377A>C
ENST00000646891.1:c.1801A>C	ENSP00000493543.1:p.Lys601Gln
ENST00000647434.1:c.738-3916A>C	ENSP00000495132.1:n.738-3916A>C
ENST00000288602.10:c.1801A>C	ENSP00000288602.6:p.Lys601Gln
ENST00000479537.5:c.85A>C	ENSP00000418033.1:p.Lys29Gln
ENST00000496384.6:c.624A>C
ENST00000497784.1:c.1836A>C	ENSP00000420119.1:n.1836A>C
NM_004333.4:c.1801A>C , LRG_299t1:c.1801A>C	NP_004324.2:p.Lys601Gln
XM_005250045.1:c.1801A>C	XP_005250102.1:p.Lys601Gln
XM_005250046.1:c.1801A>C	XP_005250103.1:p.Lys601Gln
XM_011516529.1:c.1801A>C	XP_011514831.1:p.Lys601Gln
XM_011516530.1:c.1695-3916A>C	XP_011514832.1:n.1695-3916A>C
XR_242190.1:n.1809A>C
XR_927520.1:n.1809A>C
XR_927521.1:n.1809A>C
XR_927522.1:n.1703-3916A>C
XR_927523.1:n.1703-3916A>C
NM_001354609.1:c.1801A>C	NP_001341538.1:p.Lys601Gln
NM_004333.5:c.1801A>C	NP_004324.2:p.Lys601Gln
NR_148928.1:n.2899A>C
XM_017012558.1:c.1921A>C	XP_016868047.1:p.Lys641Gln
XM_017012559.1:c.1921A>C	XP_016868048.1:p.Lys641Gln
XR_001744857.1:n.1929A>C
XR_001744858.1:n.1823-3916A>C
NM_001354609.2:c.1801A>C	NP_001341538.1:p.Lys601Gln
NM_001374244.1:c.1921A>C	NP_001361173.1:p.Lys641Gln
NM_001374258.1:c.1921A>C MANE Plus Clinical	NP_001361187.1:p.Lys641Gln
NM_004333.6:c.1801A>C MANE Select	NP_004324.2:p.Lys601Gln
NM_001378467.1:c.1810A>C	NP_001365396.1:p.Lys604Gln
NM_001378468.1:c.1801A>C	NP_001365397.1:p.Lys601Gln
NM_001378469.1:c.1735A>C	NP_001365398.1:p.Lys579Gln
NM_001378470.1:c.1699A>C	NP_001365399.1:p.Lys567Gln
NM_001378471.1:c.1690A>C	NP_001365400.1:p.Lys564Gln
NM_001378472.1:c.1645A>C	NP_001365401.1:p.Lys549Gln
NM_001378473.1:c.1645A>C	NP_001365402.1:p.Lys549Gln
NM_001378474.1:c.1801A>C	NP_001365403.1:p.Lys601Gln
NM_001378475.1:c.1537A>C	NP_001365404.1:p.Lys513Gln