Canonical Allele Identifier: CA001612

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 54564
• ClinVar RCV Id: RCV000111854 ; RCV001015485 ; RCV001194351 ; RCV001363802
• dbSNP Id: rs80357240
• gnomAD v4: 17-43093112-C-A
• MyVariant Identifiers: chr17:g.41245129C>A (hg19) ; chr17:g.43093112C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43093112C>A , CM000679.2:g.43093112C>A	GRCh38
NC_000017.10:g.41245129C>A , CM000679.1:g.41245129C>A	GRCh37
NC_000017.9:g.38498655C>A	NCBI36
NG_005905.2:g.124872G>T , LRG_292:g.124872G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.2483G>T
ENST00000461574.2:c.2419G>T	ENSP00000417241.2:p.Ala807Ser
ENST00000470026.6:c.2419G>T	ENSP00000419274.2:p.Ala807Ser
ENST00000473961.6:c.2293G>T	ENSP00000420201.2:p.Ala765Ser
ENST00000476777.6:c.2416G>T	ENSP00000417554.2:p.Ala806Ser
ENST00000477152.6:c.2341G>T	ENSP00000419988.2:p.Ala781Ser
ENST00000478531.6:c.784+1632G>T	ENSP00000420412.2:n.784+1632G>T
ENST00000489037.2:c.2341G>T	ENSP00000420781.2:p.Ala781Ser
ENST00000493919.6:c.646+1632G>T	ENSP00000418819.2:n.646+1632G>T
ENST00000494123.6:c.2419G>T	ENSP00000419103.2:p.Ala807Ser
ENST00000497488.2:c.1531G>T	ENSP00000418986.2:p.Ala511Ser
ENST00000618469.2:c.2419G>T	ENSP00000478114.2:p.Ala807Ser
ENST00000634433.2:c.2296G>T	ENSP00000489431.2:p.Ala766Ser
ENST00000644379.2:c.2419G>T	ENSP00000496570.2:p.Ala807Ser
ENST00000644555.2:c.646+1632G>T	ENSP00000494614.2:n.646+1632G>T
ENST00000652672.2:c.2278G>T	ENSP00000498906.2:p.Ala760Ser
ENST00000484087.6:c.664+1632G>T	ENSP00000419481.2:n.664+1632G>T
ENST00000700182.1:c.706+1632G>T	ENSP00000514849.1:n.706+1632G>T
ENST00000357654.9:c.2419G>T MANE Select	ENSP00000350283.3:p.Ala807Ser
ENST00000471181.7:c.2419G>T	ENSP00000418960.2:p.Ala807Ser
ENST00000352993.7:c.671-2080G>T	ENSP00000312236.5:n.671-2080G>T
ENST00000354071.7:c.2419G>T	ENSP00000326002.7:p.Ala807Ser
ENST00000357654.7:c.2419G>T	ENSP00000350283.3:p.Ala807Ser
ENST00000461221.5:c.*2202G>T	ENSP00000418548.1:n.*2202G>T
ENST00000468300.5:c.787+1632G>T	ENSP00000417148.1:n.787+1632G>T
ENST00000471181.6:c.2419G>T	ENSP00000418960.2:p.Ala807Ser
ENST00000478531.5:c.784+1632G>T	ENSP00000420412.1:n.784+1632G>T
ENST00000484087.5:c.409+1632G>T	ENSP00000419481.1:n.409+1632G>T
ENST00000487825.5:c.412+1632G>T	ENSP00000418212.1:n.412+1632G>T
ENST00000491747.6:c.787+1632G>T	ENSP00000420705.2:n.787+1632G>T
ENST00000493795.5:c.2278G>T	ENSP00000418775.1:p.Ala760Ser
ENST00000493919.5:c.646+1632G>T	ENSP00000418819.1:n.646+1632G>T
ENST00000586385.5:c.5-29161G>T	ENSP00000465818.1:n.5-29161G>T
ENST00000591534.5:c.-43-18591G>T	ENSP00000467329.1:n.-43-18591G>T
ENST00000591849.5:c.-99+32159G>T	ENSP00000465347.1:n.-99+32159G>T
ENST00000634433.1:c.2296G>T	ENSP00000489431.1:p.Ala766Ser
NM_007294.3:c.2419G>T , LRG_292t1:c.2419G>T	NP_009225.1:p.Ala807Ser
NM_007297.3:c.2278G>T	NP_009228.2:p.Ala760Ser
NM_007298.3:c.787+1632G>T	NP_009229.2:n.787+1632G>T
NM_007299.3:c.787+1632G>T	NP_009230.2:n.787+1632G>T
NM_007300.3:c.2419G>T	NP_009231.2:p.Ala807Ser
NR_027676.1:n.2555G>T
NM_007294.4:c.2419G>T MANE Select	NP_009225.1:p.Ala807Ser
NM_007297.4:c.2278G>T	NP_009228.2:p.Ala760Ser
NM_007299.4:c.787+1632G>T	NP_009230.2:n.787+1632G>T
NM_007300.4:c.2419G>T	NP_009231.2:p.Ala807Ser
NR_027676.2:n.2596G>T