Canonical Allele Identifier: CA2260760832
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43045294_43045295delinsGA , CM000679.2:g.43045294_43045295delinsGA GRCh38
NC_000017.10:g.41197311_41197312delinsGA , CM000679.1:g.41197311_41197312delinsGA GRCh37
NC_000017.9:g.38450837_38450838delinsGA NCBI36
NG_005905.2:g.172689_172690delinsTC , LRG_292:g.172689_172690delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.*383_*384delinsTC ENSP00000417241.2:n.*383_*384delinsTC
ENST00000470026.6:c.*383_*384delinsTC ENSP00000419274.2:n.*383_*384delinsTC
ENST00000473961.6:c.*383_*384delinsTC ENSP00000420201.2:n.*383_*384delinsTC
ENST00000476777.6:c.*383_*384delinsTC ENSP00000417554.2:n.*383_*384delinsTC
ENST00000477152.6:c.*383_*384delinsTC ENSP00000419988.2:n.*383_*384delinsTC
ENST00000478531.6:c.*383_*384delinsTC ENSP00000420412.2:n.*383_*384delinsTC
ENST00000489037.2:c.*383_*384delinsTC ENSP00000420781.2:n.*383_*384delinsTC
ENST00000493919.6:c.*383_*384delinsTC ENSP00000418819.2:n.*383_*384delinsTC
ENST00000494123.6:c.*383_*384delinsTC ENSP00000419103.2:n.*383_*384delinsTC
ENST00000497488.2:c.*383_*384delinsTC ENSP00000418986.2:n.*383_*384delinsTC
ENST00000618469.2:c.*383_*384delinsTC ENSP00000478114.2:n.*383_*384delinsTC
ENST00000634433.2:c.*383_*384delinsTC ENSP00000489431.2:n.*383_*384delinsTC
ENST00000644379.2:c.*383_*384delinsTC ENSP00000496570.2:n.*383_*384delinsTC
ENST00000644555.2:c.*383_*384delinsTC ENSP00000494614.2:n.*383_*384delinsTC
ENST00000652672.2:c.*383_*384delinsTC ENSP00000498906.2:n.*383_*384delinsTC
ENST00000700081.1:n.1858_1859delinsTC
ENST00000700082.1:n.1339_1340delinsTC
ENST00000357654.9:c.*383_*384delinsTC MANE Select ENSP00000350283.3:n.*383_*384delinsTC
ENST00000471181.7:c.*383_*384delinsTC ENSP00000418960.2:n.*383_*384delinsTC
ENST00000644379.1:c.2362_2363delinsTC
ENST00000352993.7:c.*383_*384delinsTC ENSP00000312236.5:n.*383_*384delinsTC
ENST00000357654.7:c.*383_*384delinsTC ENSP00000350283.3:n.*383_*384delinsTC
ENST00000468300.5:c.*489_*490delinsTC ENSP00000417148.1:n.*489_*490delinsTC
NM_007294.3:c.*383_*384delinsTC , LRG_292t1:c.*383_*384delinsTC NP_009225.1:n.*383_*384delinsTC
NM_007297.3:c.*383_*384delinsTC NP_009228.2:n.*383_*384delinsTC
NM_007298.3:c.*383_*384delinsTC NP_009229.2:n.*383_*384delinsTC
NM_007299.3:c.*489_*490delinsTC NP_009230.2:n.*489_*490delinsTC
NM_007300.3:c.*383_*384delinsTC NP_009231.2:n.*383_*384delinsTC
NR_027676.1:n.6111_6112delinsTC
NM_007294.4:c.*383_*384delinsTC MANE Select NP_009225.1:n.*383_*384delinsTC
NM_007297.4:c.*383_*384delinsTC NP_009228.2:n.*383_*384delinsTC
NM_007299.4:c.*489_*490delinsTC NP_009230.2:n.*489_*490delinsTC
NM_007300.4:c.*383_*384delinsTC NP_009231.2:n.*383_*384delinsTC
NR_027676.2:n.6152_6153delinsTC