Canonical Allele Identifier: CA10593061

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 662999
• ClinVar RCV Id: RCV000820775
• dbSNP Id: rs1597847702
• MyVariant Identifiers: chr17:g.41234447T>A (hg19) ; chr17:g.43082430T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43082430T>A , CM000679.2:g.43082430T>A	GRCh38
NC_000017.10:g.41234447T>A , CM000679.1:g.41234447T>A	GRCh37
NC_000017.9:g.38487973T>A	NCBI36
NG_005905.2:g.135554A>T , LRG_292:g.135554A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.4331A>T	ENSP00000417241.2:p.Asn1444Ile
ENST00000470026.6:c.4331A>T	ENSP00000419274.2:p.Asn1444Ile
ENST00000473961.6:c.4205A>T	ENSP00000420201.2:p.Asn1402Ile
ENST00000476777.6:c.4325A>T	ENSP00000417554.2:p.Asn1442Ile
ENST00000477152.6:c.4253A>T	ENSP00000419988.2:p.Asn1418Ile
ENST00000478531.6:c.1019A>T	ENSP00000420412.2:p.Asn340Ile
ENST00000489037.2:c.4253A>T	ENSP00000420781.2:p.Asn1418Ile
ENST00000493919.6:c.881A>T	ENSP00000418819.2:p.Asn294Ile
ENST00000494123.6:c.4331A>T	ENSP00000419103.2:p.Asn1444Ile
ENST00000497488.2:c.3443A>T	ENSP00000418986.2:p.Asn1148Ile
ENST00000618469.2:c.4331A>T	ENSP00000478114.2:p.Asn1444Ile
ENST00000634433.2:c.4208A>T	ENSP00000489431.2:p.Asn1403Ile
ENST00000644379.2:c.4331A>T	ENSP00000496570.2:p.Asn1444Ile
ENST00000644555.2:c.881A>T	ENSP00000494614.2:p.Asn294Ile
ENST00000652672.2:c.4190A>T	ENSP00000498906.2:p.Asn1397Ile
ENST00000484087.6:c.896A>T	ENSP00000419481.2:p.Asn299Ile
ENST00000700182.1:c.941A>T	ENSP00000514849.1:p.Asn314Ile
ENST00000357654.9:c.4331A>T MANE Select	ENSP00000350283.3:p.Asn1444Ile
ENST00000471181.7:c.4331A>T	ENSP00000418960.2:p.Asn1444Ile
ENST00000644379.1:c.652A>T
ENST00000352993.7:c.905A>T	ENSP00000312236.5:p.Asn302Ile
ENST00000357654.7:c.4331A>T	ENSP00000350283.3:p.Asn1444Ile
ENST00000461221.5:c.*4114A>T	ENSP00000418548.1:n.*4114A>T
ENST00000461574.1:c.625A>T
ENST00000468300.5:c.1022A>T	ENSP00000417148.1:p.Asn341Ile
ENST00000471181.6:c.4331A>T	ENSP00000418960.2:p.Asn1444Ile
ENST00000478531.5:c.1019A>T	ENSP00000420412.1:p.Asn340Ile
ENST00000484087.5:c.644A>T	ENSP00000419481.1:p.Asn215Ile
ENST00000487825.5:c.647A>T	ENSP00000418212.1:p.Asn216Ile
ENST00000491747.6:c.1022A>T	ENSP00000420705.2:p.Asn341Ile
ENST00000493795.5:c.4190A>T	ENSP00000418775.1:p.Asn1397Ile
ENST00000493919.5:c.881A>T	ENSP00000418819.1:p.Asn294Ile
ENST00000586385.5:c.5-18479A>T	ENSP00000465818.1:n.5-18479A>T
ENST00000591534.5:c.-43-7909A>T	ENSP00000467329.1:n.-43-7909A>T
ENST00000591849.5:c.-98-32240A>T	ENSP00000465347.1:n.-98-32240A>T
ENST00000621897.1:n.225A>T
NM_007294.3:c.4331A>T , LRG_292t1:c.4331A>T	NP_009225.1:p.Asn1444Ile
NM_007297.3:c.4190A>T	NP_009228.2:p.Asn1397Ile
NM_007298.3:c.1022A>T	NP_009229.2:p.Asn341Ile
NM_007299.3:c.1022A>T	NP_009230.2:p.Asn341Ile
NM_007300.3:c.4331A>T	NP_009231.2:p.Asn1444Ile
NR_027676.1:n.4467A>T
NM_007294.4:c.4331A>T MANE Select	NP_009225.1:p.Asn1444Ile
NM_007297.4:c.4190A>T	NP_009228.2:p.Asn1397Ile
NM_007299.4:c.1022A>T	NP_009230.2:p.Asn341Ile
NM_007300.4:c.4331A>T	NP_009231.2:p.Asn1444Ile
NR_027676.2:n.4508A>T