Canonical Allele Identifier: CA10591654

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 868859
• ClinVar RCV Id: RCV001077845
• dbSNP Id: rs2052371775
• gnomAD v4: 17-43070978-C-T
• MyVariant Identifiers: chr17:g.41222995C>T (hg19) ; chr17:g.43070978C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43070978C>T , CM000679.2:g.43070978C>T	GRCh38
NC_000017.10:g.41222995C>T , CM000679.1:g.41222995C>T	GRCh37
NC_000017.9:g.38476521C>T	NCBI36
NG_005905.2:g.147006G>A , LRG_292:g.147006G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000461574.2:c.4933G>A	ENSP00000417241.2:p.Val1645Ile
ENST00000470026.6:c.4936G>A	ENSP00000419274.2:p.Val1646Ile
ENST00000473961.6:c.4810G>A	ENSP00000420201.2:p.Val1604Ile
ENST00000476777.6:c.4930G>A	ENSP00000417554.2:p.Val1644Ile
ENST00000477152.6:c.4858G>A	ENSP00000419988.2:p.Val1620Ile
ENST00000478531.6:c.1624G>A	ENSP00000420412.2:p.Val542Ile
ENST00000489037.2:c.4858G>A	ENSP00000420781.2:p.Val1620Ile
ENST00000493919.6:c.1486G>A	ENSP00000418819.2:p.Val496Ile
ENST00000494123.6:c.4936G>A	ENSP00000419103.2:p.Val1646Ile
ENST00000497488.2:c.4048G>A	ENSP00000418986.2:p.Val1350Ile
ENST00000618469.2:c.4936G>A	ENSP00000478114.2:p.Val1646Ile
ENST00000634433.2:c.4813G>A	ENSP00000489431.2:p.Val1605Ile
ENST00000644379.2:c.5002G>A	ENSP00000496570.2:p.Val1668Ile
ENST00000644555.2:c.1486G>A	ENSP00000494614.2:p.Val496Ile
ENST00000652672.2:c.4795G>A	ENSP00000498906.2:p.Val1599Ile
ENST00000484087.6:c.1498G>A	ENSP00000419481.2:p.Val500Ile
ENST00000700182.1:c.1543G>A	ENSP00000514849.1:p.Val515Ile
ENST00000357654.9:c.4936G>A MANE Select	ENSP00000350283.3:p.Val1646Ile
ENST00000471181.7:c.4999G>A	ENSP00000418960.2:p.Val1667Ile
ENST00000644379.1:c.1323G>A
ENST00000352993.7:c.1510G>A	ENSP00000312236.5:p.Val504Ile
ENST00000357654.7:c.4936G>A	ENSP00000350283.3:p.Val1646Ile
ENST00000461221.5:c.*4719G>A	ENSP00000418548.1:n.*4719G>A
ENST00000468300.5:c.1624G>A	ENSP00000417148.1:p.Val542Ile
ENST00000471181.6:c.4999G>A	ENSP00000418960.2:p.Val1667Ile
ENST00000472490.1:n.89G>A
ENST00000478531.5:c.1624G>A	ENSP00000420412.1:p.Val542Ile
ENST00000484087.5:c.1249G>A	ENSP00000419481.1:p.Val417Ile
ENST00000491747.6:c.1624G>A	ENSP00000420705.2:p.Val542Ile
ENST00000493795.5:c.4795G>A	ENSP00000418775.1:p.Val1599Ile
ENST00000493919.5:c.1486G>A	ENSP00000418819.1:p.Val496Ile
ENST00000586385.5:c.5-7027G>A	ENSP00000465818.1:n.5-7027G>A
ENST00000591534.5:c.409G>A	ENSP00000467329.1:p.Val137Ile
ENST00000591849.5:c.-98-20788G>A	ENSP00000465347.1:n.-98-20788G>A
NM_007294.3:c.4936G>A , LRG_292t1:c.4936G>A	NP_009225.1:p.Val1646Ile
NM_007297.3:c.4795G>A	NP_009228.2:p.Val1599Ile
NM_007298.3:c.1624G>A	NP_009229.2:p.Val542Ile
NM_007299.3:c.1624G>A	NP_009230.2:p.Val542Ile
NM_007300.3:c.4999G>A	NP_009231.2:p.Val1667Ile
NR_027676.1:n.5072G>A
NM_007294.4:c.4936G>A MANE Select	NP_009225.1:p.Val1646Ile
NM_007297.4:c.4795G>A	NP_009228.2:p.Val1599Ile
NM_007299.4:c.1624G>A	NP_009230.2:p.Val542Ile
NM_007300.4:c.4999G>A	NP_009231.2:p.Val1667Ile
NR_027676.2:n.5113G>A