Canonical Allele Identifier: CA10596116

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 531238
• ClinVar RCV Id: RCV000637395 ; RCV002258980
• dbSNP Id: rs1555588677
• gnomAD v4: 17-43092590-G-T
• MyVariant Identifiers: chr17:g.41244607G>T (hg19) ; chr17:g.43092590G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43092590G>T , CM000679.2:g.43092590G>T	GRCh38
NC_000017.10:g.41244607G>T , CM000679.1:g.41244607G>T	GRCh37
NC_000017.9:g.38498133G>T	NCBI36
NG_005905.2:g.125394C>A , LRG_292:g.125394C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.3005C>A
ENST00000461574.2:c.2941C>A	ENSP00000417241.2:p.Pro981Thr
ENST00000470026.6:c.2941C>A	ENSP00000419274.2:p.Pro981Thr
ENST00000473961.6:c.2815C>A	ENSP00000420201.2:p.Pro939Thr
ENST00000476777.6:c.2938C>A	ENSP00000417554.2:p.Pro980Thr
ENST00000477152.6:c.2863C>A	ENSP00000419988.2:p.Pro955Thr
ENST00000478531.6:c.785-1558C>A	ENSP00000420412.2:n.785-1558C>A
ENST00000489037.2:c.2863C>A	ENSP00000420781.2:p.Pro955Thr
ENST00000493919.6:c.647-1558C>A	ENSP00000418819.2:n.647-1558C>A
ENST00000494123.6:c.2941C>A	ENSP00000419103.2:p.Pro981Thr
ENST00000497488.2:c.2053C>A	ENSP00000418986.2:p.Pro685Thr
ENST00000618469.2:c.2941C>A	ENSP00000478114.2:p.Pro981Thr
ENST00000634433.2:c.2818C>A	ENSP00000489431.2:p.Pro940Thr
ENST00000644379.2:c.2941C>A	ENSP00000496570.2:p.Pro981Thr
ENST00000644555.2:c.647-1558C>A	ENSP00000494614.2:n.647-1558C>A
ENST00000652672.2:c.2800C>A	ENSP00000498906.2:p.Pro934Thr
ENST00000484087.6:c.665-1558C>A	ENSP00000419481.2:n.665-1558C>A
ENST00000700182.1:c.707-1558C>A	ENSP00000514849.1:n.707-1558C>A
ENST00000357654.9:c.2941C>A MANE Select	ENSP00000350283.3:p.Pro981Thr
ENST00000471181.7:c.2941C>A	ENSP00000418960.2:p.Pro981Thr
ENST00000352993.7:c.671-1558C>A	ENSP00000312236.5:n.671-1558C>A
ENST00000354071.7:c.2941C>A	ENSP00000326002.7:p.Pro981Thr
ENST00000357654.7:c.2941C>A	ENSP00000350283.3:p.Pro981Thr
ENST00000461221.5:c.*2724C>A	ENSP00000418548.1:n.*2724C>A
ENST00000468300.5:c.788-1558C>A	ENSP00000417148.1:n.788-1558C>A
ENST00000471181.6:c.2941C>A	ENSP00000418960.2:p.Pro981Thr
ENST00000478531.5:c.785-1558C>A	ENSP00000420412.1:n.785-1558C>A
ENST00000484087.5:c.410-1558C>A	ENSP00000419481.1:n.410-1558C>A
ENST00000487825.5:c.413-1558C>A	ENSP00000418212.1:n.413-1558C>A
ENST00000491747.6:c.788-1558C>A	ENSP00000420705.2:n.788-1558C>A
ENST00000493795.5:c.2800C>A	ENSP00000418775.1:p.Pro934Thr
ENST00000493919.5:c.647-1558C>A	ENSP00000418819.1:n.647-1558C>A
ENST00000586385.5:c.5-28639C>A	ENSP00000465818.1:n.5-28639C>A
ENST00000591534.5:c.-43-18069C>A	ENSP00000467329.1:n.-43-18069C>A
ENST00000591849.5:c.-99+32681C>A	ENSP00000465347.1:n.-99+32681C>A
NM_007294.3:c.2941C>A , LRG_292t1:c.2941C>A	NP_009225.1:p.Pro981Thr
NM_007297.3:c.2800C>A	NP_009228.2:p.Pro934Thr
NM_007298.3:c.788-1558C>A	NP_009229.2:n.788-1558C>A
NM_007299.3:c.788-1558C>A	NP_009230.2:n.788-1558C>A
NM_007300.3:c.2941C>A	NP_009231.2:p.Pro981Thr
NR_027676.1:n.3077C>A
NM_007294.4:c.2941C>A MANE Select	NP_009225.1:p.Pro981Thr
NM_007297.4:c.2800C>A	NP_009228.2:p.Pro934Thr
NM_007299.4:c.788-1558C>A	NP_009230.2:n.788-1558C>A
NM_007300.4:c.2941C>A	NP_009231.2:p.Pro981Thr
NR_027676.2:n.3118C>A