Canonical Allele Identifier: CA983864945
Gene: BRCA1 HGNC NCBI

Linked Data

dbSNP Id: rs2050835305

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43045322C>T , CM000679.2:g.43045322C>T GRCh38
NC_000017.10:g.41197339C>T , CM000679.1:g.41197339C>T GRCh37
NC_000017.9:g.38450865C>T NCBI36
NG_005905.2:g.172662G>A , LRG_292:g.172662G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.*356G>A ENSP00000417241.2:n.*356G>A
ENST00000470026.6:c.*356G>A ENSP00000419274.2:n.*356G>A
ENST00000473961.6:c.*356G>A ENSP00000420201.2:n.*356G>A
ENST00000476777.6:c.*356G>A ENSP00000417554.2:n.*356G>A
ENST00000477152.6:c.*356G>A ENSP00000419988.2:n.*356G>A
ENST00000478531.6:c.*356G>A ENSP00000420412.2:n.*356G>A
ENST00000489037.2:c.*356G>A ENSP00000420781.2:n.*356G>A
ENST00000493919.6:c.*356G>A ENSP00000418819.2:n.*356G>A
ENST00000494123.6:c.*356G>A ENSP00000419103.2:n.*356G>A
ENST00000497488.2:c.*356G>A ENSP00000418986.2:n.*356G>A
ENST00000618469.2:c.*356G>A ENSP00000478114.2:n.*356G>A
ENST00000634433.2:c.*356G>A ENSP00000489431.2:n.*356G>A
ENST00000644379.2:c.*356G>A ENSP00000496570.2:n.*356G>A
ENST00000644555.2:c.*356G>A ENSP00000494614.2:n.*356G>A
ENST00000652672.2:c.*356G>A ENSP00000498906.2:n.*356G>A
ENST00000700081.1:n.1831G>A
ENST00000700082.1:n.1312G>A
ENST00000357654.9:c.*356G>A MANE Select ENSP00000350283.3:n.*356G>A
ENST00000471181.7:c.*356G>A ENSP00000418960.2:n.*356G>A
ENST00000644379.1:c.2335G>A
ENST00000352993.7:c.*356G>A ENSP00000312236.5:n.*356G>A
ENST00000357654.7:c.*356G>A ENSP00000350283.3:n.*356G>A
ENST00000468300.5:c.*462G>A ENSP00000417148.1:n.*462G>A
NM_007294.3:c.*356G>A , LRG_292t1:c.*356G>A NP_009225.1:n.*356G>A
NM_007297.3:c.*356G>A NP_009228.2:n.*356G>A
NM_007298.3:c.*356G>A NP_009229.2:n.*356G>A
NM_007299.3:c.*462G>A NP_009230.2:n.*462G>A
NM_007300.3:c.*356G>A NP_009231.2:n.*356G>A
NR_027676.1:n.6084G>A
NM_007294.4:c.*356G>A MANE Select NP_009225.1:n.*356G>A
NM_007297.4:c.*356G>A NP_009228.2:n.*356G>A
NM_007299.4:c.*462G>A NP_009230.2:n.*462G>A
NM_007300.4:c.*356G>A NP_009231.2:n.*356G>A
NR_027676.2:n.6125G>A