Canonical Allele Identifier: CA2733917094
Gene: BRCA1 HGNC NCBI

Linked Data

dbSNP Id: rs2152615672

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43045829T>G , CM000679.2:g.43045829T>G GRCh38
NC_000017.10:g.41197846T>G , CM000679.1:g.41197846T>G GRCh37
NC_000017.9:g.38451372T>G NCBI36
NG_005905.2:g.172155A>C , LRG_292:g.172155A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5465-27A>C ENSP00000417241.2:n.5465-27A>C
ENST00000470026.6:c.5468-27A>C ENSP00000419274.2:n.5468-27A>C
ENST00000473961.6:c.5342-27A>C ENSP00000420201.2:n.5342-27A>C
ENST00000476777.6:c.5462-27A>C ENSP00000417554.2:n.5462-27A>C
ENST00000477152.6:c.5390-27A>C ENSP00000419988.2:n.5390-27A>C
ENST00000478531.6:c.2156-27A>C ENSP00000420412.2:n.2156-27A>C
ENST00000489037.2:c.5390-27A>C ENSP00000420781.2:n.5390-27A>C
ENST00000493919.6:c.2018-27A>C ENSP00000418819.2:n.2018-27A>C
ENST00000494123.6:c.5468-27A>C ENSP00000419103.2:n.5468-27A>C
ENST00000497488.2:c.4580-27A>C ENSP00000418986.2:n.4580-27A>C
ENST00000618469.2:c.5468-27A>C ENSP00000478114.2:n.5468-27A>C
ENST00000634433.2:c.5345-27A>C ENSP00000489431.2:n.5345-27A>C
ENST00000644379.2:c.5534-27A>C ENSP00000496570.2:n.5534-27A>C
ENST00000644555.2:c.2018-27A>C ENSP00000494614.2:n.2018-27A>C
ENST00000652672.2:c.5327-27A>C ENSP00000498906.2:n.5327-27A>C
ENST00000484087.6:c.2030-27A>C ENSP00000419481.2:n.2030-27A>C
ENST00000700081.1:n.1351-27A>C
ENST00000700082.1:n.832-27A>C
ENST00000357654.9:c.5468-27A>C MANE Select ENSP00000350283.3:n.5468-27A>C
ENST00000471181.7:c.5531-27A>C ENSP00000418960.2:n.5531-27A>C
ENST00000644379.1:c.1855-27A>C
ENST00000352993.7:c.2042-27A>C ENSP00000312236.5:n.2042-27A>C
ENST00000357654.7:c.5468-27A>C ENSP00000350283.3:n.5468-27A>C
ENST00000461221.5:c.*5251-27A>C ENSP00000418548.1:n.*5251-27A>C
ENST00000468300.5:c.2082-27A>C ENSP00000417148.1:n.2082-27A>C
ENST00000471181.6:c.5531-27A>C ENSP00000418960.2:n.5531-27A>C
ENST00000491747.6:c.2156-27A>C ENSP00000420705.2:n.2156-27A>C
ENST00000493795.5:c.5327-27A>C ENSP00000418775.1:n.5327-27A>C
ENST00000586385.5:c.398-27A>C ENSP00000465818.1:n.398-27A>C
ENST00000591534.5:c.941-27A>C ENSP00000467329.1:n.941-27A>C
ENST00000591849.5:c.167-27A>C ENSP00000465347.1:n.167-27A>C
NM_007294.3:c.5468-27A>C , LRG_292t1:c.5468-27A>C NP_009225.1:n.5468-27A>C
NM_007297.3:c.5327-27A>C NP_009228.2:n.5327-27A>C
NM_007298.3:c.2156-27A>C NP_009229.2:n.2156-27A>C
NM_007299.3:c.2082-27A>C NP_009230.2:n.2082-27A>C
NM_007300.3:c.5531-27A>C NP_009231.2:n.5531-27A>C
NR_027676.1:n.5604-27A>C
NM_007294.4:c.5468-27A>C MANE Select NP_009225.1:n.5468-27A>C
NM_007297.4:c.5327-27A>C NP_009228.2:n.5327-27A>C
NM_007299.4:c.2082-27A>C NP_009230.2:n.2082-27A>C
NM_007300.4:c.5531-27A>C NP_009231.2:n.5531-27A>C
NR_027676.2:n.5645-27A>C