Canonical Allele Identifier: CA772163847
Gene: BRCA1 HGNC NCBI

Linked Data

dbSNP Id: rs1357432929

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43045340dup , CM000679.2:g.43045340dup GRCh38
NC_000017.10:g.41197357dup , CM000679.1:g.41197357dup GRCh37
NC_000017.9:g.38450883dup NCBI36
NG_005905.2:g.172646dup , LRG_292:g.172646dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.*340dup ENSP00000417241.2:n.*340dup
ENST00000470026.6:c.*340dup ENSP00000419274.2:n.*340dup
ENST00000473961.6:c.*340dup ENSP00000420201.2:n.*340dup
ENST00000476777.6:c.*340dup ENSP00000417554.2:n.*340dup
ENST00000477152.6:c.*340dup ENSP00000419988.2:n.*340dup
ENST00000478531.6:c.*340dup ENSP00000420412.2:n.*340dup
ENST00000489037.2:c.*340dup ENSP00000420781.2:n.*340dup
ENST00000493919.6:c.*340dup ENSP00000418819.2:n.*340dup
ENST00000494123.6:c.*340dup ENSP00000419103.2:n.*340dup
ENST00000497488.2:c.*340dup ENSP00000418986.2:n.*340dup
ENST00000618469.2:c.*340dup ENSP00000478114.2:n.*340dup
ENST00000634433.2:c.*340dup ENSP00000489431.2:n.*340dup
ENST00000644379.2:c.*340dup ENSP00000496570.2:n.*340dup
ENST00000644555.2:c.*340dup ENSP00000494614.2:n.*340dup
ENST00000652672.2:c.*340dup ENSP00000498906.2:n.*340dup
ENST00000700081.1:n.1815dup
ENST00000700082.1:n.1296dup
ENST00000357654.9:c.*340dup MANE Select ENSP00000350283.3:n.*340dup
ENST00000471181.7:c.*340dup ENSP00000418960.2:n.*340dup
ENST00000644379.1:c.2319dup
ENST00000352993.7:c.*340dup ENSP00000312236.5:n.*340dup
ENST00000357654.7:c.*340dup ENSP00000350283.3:n.*340dup
ENST00000468300.5:c.*446dup ENSP00000417148.1:n.*446dup
NM_007294.3:c.*340dup , LRG_292t1:c.*340dup NP_009225.1:n.*340dup
NM_007297.3:c.*340dup NP_009228.2:n.*340dup
NM_007298.3:c.*340dup NP_009229.2:n.*340dup
NM_007299.3:c.*446dup NP_009230.2:n.*446dup
NM_007300.3:c.*340dup NP_009231.2:n.*340dup
NR_027676.1:n.6068dup
NM_007294.4:c.*340dup MANE Select NP_009225.1:n.*340dup
NM_007297.4:c.*340dup NP_009228.2:n.*340dup
NM_007299.4:c.*446dup NP_009230.2:n.*446dup
NM_007300.4:c.*340dup NP_009231.2:n.*340dup
NR_027676.2:n.6109dup