Canonical Allele Identifier: CA2260761540
Gene: BRCA1 HGNC NCBI

Linked Data

dbSNP Id: rs2050930472

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43046677C>T , CM000679.2:g.43046677C>T GRCh38
NC_000017.10:g.41198694C>T , CM000679.1:g.41198694C>T GRCh37
NC_000017.9:g.38452220C>T NCBI36
NG_005905.2:g.171307G>A , LRG_292:g.171307G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000461574.2:c.5465-875G>A ENSP00000417241.2:n.5465-875G>A
ENST00000470026.6:c.5468-875G>A ENSP00000419274.2:n.5468-875G>A
ENST00000473961.6:c.5342-875G>A ENSP00000420201.2:n.5342-875G>A
ENST00000476777.6:c.5462-875G>A ENSP00000417554.2:n.5462-875G>A
ENST00000477152.6:c.5390-875G>A ENSP00000419988.2:n.5390-875G>A
ENST00000478531.6:c.2156-875G>A ENSP00000420412.2:n.2156-875G>A
ENST00000489037.2:c.5390-875G>A ENSP00000420781.2:n.5390-875G>A
ENST00000493919.6:c.2018-875G>A ENSP00000418819.2:n.2018-875G>A
ENST00000494123.6:c.5468-875G>A ENSP00000419103.2:n.5468-875G>A
ENST00000497488.2:c.4580-875G>A ENSP00000418986.2:n.4580-875G>A
ENST00000618469.2:c.5468-875G>A ENSP00000478114.2:n.5468-875G>A
ENST00000634433.2:c.5345-875G>A ENSP00000489431.2:n.5345-875G>A
ENST00000644379.2:c.5534-875G>A ENSP00000496570.2:n.5534-875G>A
ENST00000644555.2:c.2018-875G>A ENSP00000494614.2:n.2018-875G>A
ENST00000652672.2:c.5327-875G>A ENSP00000498906.2:n.5327-875G>A
ENST00000484087.6:c.2030-875G>A ENSP00000419481.2:n.2030-875G>A
ENST00000700081.1:n.1351-875G>A
ENST00000700082.1:n.832-875G>A
ENST00000357654.9:c.5468-875G>A MANE Select ENSP00000350283.3:n.5468-875G>A
ENST00000471181.7:c.5531-875G>A ENSP00000418960.2:n.5531-875G>A
ENST00000644379.1:c.1855-875G>A
ENST00000352993.7:c.2042-875G>A ENSP00000312236.5:n.2042-875G>A
ENST00000357654.7:c.5468-875G>A ENSP00000350283.3:n.5468-875G>A
ENST00000461221.5:c.*5251-875G>A ENSP00000418548.1:n.*5251-875G>A
ENST00000468300.5:c.2082-875G>A ENSP00000417148.1:n.2082-875G>A
ENST00000471181.6:c.5531-875G>A ENSP00000418960.2:n.5531-875G>A
ENST00000491747.6:c.2156-875G>A ENSP00000420705.2:n.2156-875G>A
ENST00000493795.5:c.5327-875G>A ENSP00000418775.1:n.5327-875G>A
ENST00000586385.5:c.398-875G>A ENSP00000465818.1:n.398-875G>A
ENST00000591534.5:c.941-875G>A ENSP00000467329.1:n.941-875G>A
ENST00000591849.5:c.167-875G>A ENSP00000465347.1:n.167-875G>A
NM_007294.3:c.5468-875G>A , LRG_292t1:c.5468-875G>A NP_009225.1:n.5468-875G>A
NM_007297.3:c.5327-875G>A NP_009228.2:n.5327-875G>A
NM_007298.3:c.2156-875G>A NP_009229.2:n.2156-875G>A
NM_007299.3:c.2082-875G>A NP_009230.2:n.2082-875G>A
NM_007300.3:c.5531-875G>A NP_009231.2:n.5531-875G>A
NR_027676.1:n.5604-875G>A
NM_007294.4:c.5468-875G>A MANE Select NP_009225.1:n.5468-875G>A
NM_007297.4:c.5327-875G>A NP_009228.2:n.5327-875G>A
NM_007299.4:c.2082-875G>A NP_009230.2:n.2082-875G>A
NM_007300.4:c.5531-875G>A NP_009231.2:n.5531-875G>A
NR_027676.2:n.5645-875G>A