Canonical Allele Identifier: CA10591480

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 419497
• ClinVar RCV Id: RCV000481622 ; RCV001023427 ; RCV001072978 ; RCV001851165
• dbSNP Id: rs1064793913
• MyVariant Identifiers: chr17:g.41219681T>C (hg19) ; chr17:g.43067664T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43067664T>C , CM000679.2:g.43067664T>C	GRCh38
NC_000017.10:g.41219681T>C , CM000679.1:g.41219681T>C	GRCh37
NC_000017.9:g.38473207T>C	NCBI36
NG_005905.2:g.150320A>G , LRG_292:g.150320A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.5015A>G	ENSP00000417241.2:p.His1672Arg
ENST00000470026.6:c.5018A>G	ENSP00000419274.2:p.His1673Arg
ENST00000473961.6:c.4892A>G	ENSP00000420201.2:p.His1631Arg
ENST00000476777.6:c.5012A>G	ENSP00000417554.2:p.His1671Arg
ENST00000477152.6:c.4940A>G	ENSP00000419988.2:p.His1647Arg
ENST00000478531.6:c.1706A>G	ENSP00000420412.2:p.His569Arg
ENST00000489037.2:c.4940A>G	ENSP00000420781.2:p.His1647Arg
ENST00000493919.6:c.1568A>G	ENSP00000418819.2:p.His523Arg
ENST00000494123.6:c.5018A>G	ENSP00000419103.2:p.His1673Arg
ENST00000497488.2:c.4130A>G	ENSP00000418986.2:p.His1377Arg
ENST00000618469.2:c.5018A>G	ENSP00000478114.2:p.His1673Arg
ENST00000634433.2:c.4895A>G	ENSP00000489431.2:p.His1632Arg
ENST00000644379.2:c.5084A>G	ENSP00000496570.2:p.His1695Arg
ENST00000644555.2:c.1568A>G	ENSP00000494614.2:p.His523Arg
ENST00000652672.2:c.4877A>G	ENSP00000498906.2:p.His1626Arg
ENST00000484087.6:c.1580A>G	ENSP00000419481.2:p.His527Arg
ENST00000357654.9:c.5018A>G MANE Select	ENSP00000350283.3:p.His1673Arg
ENST00000471181.7:c.5081A>G	ENSP00000418960.2:p.His1694Arg
ENST00000644379.1:c.1405A>G
ENST00000352993.7:c.1592A>G	ENSP00000312236.5:p.His531Arg
ENST00000357654.7:c.5018A>G	ENSP00000350283.3:p.His1673Arg
ENST00000461221.5:c.*4801A>G	ENSP00000418548.1:n.*4801A>G
ENST00000468300.5:c.1706A>G	ENSP00000417148.1:p.His569Arg
ENST00000471181.6:c.5081A>G	ENSP00000418960.2:p.His1694Arg
ENST00000472490.1:n.171A>G
ENST00000478531.5:c.1706A>G	ENSP00000420412.1:p.His569Arg
ENST00000484087.5:c.1331A>G	ENSP00000419481.1:p.His444Arg
ENST00000491747.6:c.1706A>G	ENSP00000420705.2:p.His569Arg
ENST00000493795.5:c.4877A>G	ENSP00000418775.1:p.His1626Arg
ENST00000493919.5:c.1568A>G	ENSP00000418819.1:p.His523Arg
ENST00000586385.5:c.5-3713A>G	ENSP00000465818.1:n.5-3713A>G
ENST00000591534.5:c.491A>G	ENSP00000467329.1:p.His164Arg
ENST00000591849.5:c.-98-17474A>G	ENSP00000465347.1:n.-98-17474A>G
NM_007294.3:c.5018A>G , LRG_292t1:c.5018A>G	NP_009225.1:p.His1673Arg
NM_007297.3:c.4877A>G	NP_009228.2:p.His1626Arg
NM_007298.3:c.1706A>G	NP_009229.2:p.His569Arg
NM_007299.3:c.1706A>G	NP_009230.2:p.His569Arg
NM_007300.3:c.5081A>G	NP_009231.2:p.His1694Arg
NR_027676.1:n.5154A>G
NM_007294.4:c.5018A>G MANE Select	NP_009225.1:p.His1673Arg
NM_007297.4:c.4877A>G	NP_009228.2:p.His1626Arg
NM_007299.4:c.1706A>G	NP_009230.2:p.His569Arg
NM_007300.4:c.5081A>G	NP_009231.2:p.His1694Arg
NR_027676.2:n.5195A>G