Canonical Allele Identifier: CA10591507

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 865523
• ClinVar RCV Id: RCV001072960
• dbSNP Id: rs1057518640
• MyVariant Identifiers: chr17:g.41219693G>C (hg19) ; chr17:g.43067676G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43067676G>C , CM000679.2:g.43067676G>C	GRCh38
NC_000017.10:g.41219693G>C , CM000679.1:g.41219693G>C	GRCh37
NC_000017.9:g.38473219G>C	NCBI36
NG_005905.2:g.150308C>G , LRG_292:g.150308C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.5003C>G	ENSP00000417241.2:p.Ala1668Gly
ENST00000470026.6:c.5006C>G	ENSP00000419274.2:p.Ala1669Gly
ENST00000473961.6:c.4880C>G	ENSP00000420201.2:p.Ala1627Gly
ENST00000476777.6:c.5000C>G	ENSP00000417554.2:p.Ala1667Gly
ENST00000477152.6:c.4928C>G	ENSP00000419988.2:p.Ala1643Gly
ENST00000478531.6:c.1694C>G	ENSP00000420412.2:p.Ala565Gly
ENST00000489037.2:c.4928C>G	ENSP00000420781.2:p.Ala1643Gly
ENST00000493919.6:c.1556C>G	ENSP00000418819.2:p.Ala519Gly
ENST00000494123.6:c.5006C>G	ENSP00000419103.2:p.Ala1669Gly
ENST00000497488.2:c.4118C>G	ENSP00000418986.2:p.Ala1373Gly
ENST00000618469.2:c.5006C>G	ENSP00000478114.2:p.Ala1669Gly
ENST00000634433.2:c.4883C>G	ENSP00000489431.2:p.Ala1628Gly
ENST00000644379.2:c.5072C>G	ENSP00000496570.2:p.Ala1691Gly
ENST00000644555.2:c.1556C>G	ENSP00000494614.2:p.Ala519Gly
ENST00000652672.2:c.4865C>G	ENSP00000498906.2:p.Ala1622Gly
ENST00000484087.6:c.1568C>G	ENSP00000419481.2:p.Ala523Gly
ENST00000357654.9:c.5006C>G MANE Select	ENSP00000350283.3:p.Ala1669Gly
ENST00000471181.7:c.5069C>G	ENSP00000418960.2:p.Ala1690Gly
ENST00000644379.1:c.1393C>G
ENST00000352993.7:c.1580C>G	ENSP00000312236.5:p.Ala527Gly
ENST00000357654.7:c.5006C>G	ENSP00000350283.3:p.Ala1669Gly
ENST00000461221.5:c.*4789C>G	ENSP00000418548.1:n.*4789C>G
ENST00000468300.5:c.1694C>G	ENSP00000417148.1:p.Ala565Gly
ENST00000471181.6:c.5069C>G	ENSP00000418960.2:p.Ala1690Gly
ENST00000472490.1:n.159C>G
ENST00000478531.5:c.1694C>G	ENSP00000420412.1:p.Ala565Gly
ENST00000484087.5:c.1319C>G	ENSP00000419481.1:p.Ala440Gly
ENST00000491747.6:c.1694C>G	ENSP00000420705.2:p.Ala565Gly
ENST00000493795.5:c.4865C>G	ENSP00000418775.1:p.Ala1622Gly
ENST00000493919.5:c.1556C>G	ENSP00000418819.1:p.Ala519Gly
ENST00000586385.5:c.5-3725C>G	ENSP00000465818.1:n.5-3725C>G
ENST00000591534.5:c.479C>G	ENSP00000467329.1:p.Ala160Gly
ENST00000591849.5:c.-98-17486C>G	ENSP00000465347.1:n.-98-17486C>G
NM_007294.3:c.5006C>G , LRG_292t1:c.5006C>G	NP_009225.1:p.Ala1669Gly
NM_007297.3:c.4865C>G	NP_009228.2:p.Ala1622Gly
NM_007298.3:c.1694C>G	NP_009229.2:p.Ala565Gly
NM_007299.3:c.1694C>G	NP_009230.2:p.Ala565Gly
NM_007300.3:c.5069C>G	NP_009231.2:p.Ala1690Gly
NR_027676.1:n.5142C>G
NM_007294.4:c.5006C>G MANE Select	NP_009225.1:p.Ala1669Gly
NM_007297.4:c.4865C>G	NP_009228.2:p.Ala1622Gly
NM_007299.4:c.1694C>G	NP_009230.2:p.Ala565Gly
NM_007300.4:c.5069C>G	NP_009231.2:p.Ala1690Gly
NR_027676.2:n.5183C>G