Canonical Allele Identifier: CA2260782005
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43091525_43091529delinsTCAGA , CM000679.2:g.43091525_43091529delinsTCAGA GRCh38
NC_000017.10:g.41243542_41243546delinsTCAGA , CM000679.1:g.41243542_41243546delinsTCAGA GRCh37
NC_000017.9:g.38497068_38497072delinsTCAGA NCBI36
NG_005905.2:g.126455_126459delinsTCTGA , LRG_292:g.126455_126459delinsTCTGA

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.4066_4070delinsTCTGA
ENST00000461574.2:c.4002_4006delinsTCTGA ENSP00000417241.2:p.Gly1334=
ENST00000470026.6:c.4002_4006delinsTCTGA ENSP00000419274.2:p.Gly1334=
ENST00000473961.6:c.3876_3880delinsTCTGA ENSP00000420201.2:p.Gly1292=
ENST00000476777.6:c.3999_4003delinsTCTGA ENSP00000417554.2:p.Gly1333=
ENST00000477152.6:c.3924_3928delinsTCTGA ENSP00000419988.2:p.Gly1308=
ENST00000478531.6:c.785-497_785-493delinsTCTGA ENSP00000420412.2:n.785-497_785-493delinsTCTGA
ENST00000489037.2:c.3924_3928delinsTCTGA ENSP00000420781.2:p.Gly1308=
ENST00000493919.6:c.647-497_647-493delinsTCTGA ENSP00000418819.2:n.647-497_647-493delinsTCTGA
ENST00000494123.6:c.4002_4006delinsTCTGA ENSP00000419103.2:p.Gly1334=
ENST00000497488.2:c.3114_3118delinsTCTGA ENSP00000418986.2:p.Gly1038=
ENST00000618469.2:c.4002_4006delinsTCTGA ENSP00000478114.2:p.Gly1334=
ENST00000634433.2:c.3879_3883delinsTCTGA ENSP00000489431.2:p.Gly1293=
ENST00000644379.2:c.4002_4006delinsTCTGA ENSP00000496570.2:p.Gly1334=
ENST00000644555.2:c.647-497_647-493delinsTCTGA ENSP00000494614.2:n.647-497_647-493delinsTCTGA
ENST00000652672.2:c.3861_3865delinsTCTGA ENSP00000498906.2:p.Gly1287=
ENST00000484087.6:c.665-497_665-493delinsTCTGA ENSP00000419481.2:n.665-497_665-493delinsTCTGA
ENST00000700182.1:c.707-497_707-493delinsTCTGA ENSP00000514849.1:n.707-497_707-493delinsTCTGA
ENST00000357654.9:c.4002_4006delinsTCTGA MANE Select ENSP00000350283.3:p.Gly1334=
ENST00000471181.7:c.4002_4006delinsTCTGA ENSP00000418960.2:p.Gly1334=
ENST00000644379.1:c.323_327delinsTCTGA
ENST00000352993.7:c.671-497_671-493delinsTCTGA ENSP00000312236.5:n.671-497_671-493delinsTCTGA
ENST00000354071.7:c.4002_4006delinsTCTGA ENSP00000326002.7:p.Gly1334=
ENST00000357654.7:c.4002_4006delinsTCTGA ENSP00000350283.3:p.Gly1334=
ENST00000461221.5:c.*3785_*3789delinsTCTGA ENSP00000418548.1:n.*3785_*3789delinsTCTGA
ENST00000461574.1:c.296_300delinsTCTGA
ENST00000468300.5:c.788-497_788-493delinsTCTGA ENSP00000417148.1:n.788-497_788-493delinsTCTGA
ENST00000471181.6:c.4002_4006delinsTCTGA ENSP00000418960.2:p.Gly1334=
ENST00000478531.5:c.785-497_785-493delinsTCTGA ENSP00000420412.1:n.785-497_785-493delinsTCTGA
ENST00000484087.5:c.410-497_410-493delinsTCTGA ENSP00000419481.1:n.410-497_410-493delinsTCTGA
ENST00000487825.5:c.413-497_413-493delinsTCTGA ENSP00000418212.1:n.413-497_413-493delinsTCTGA
ENST00000491747.6:c.788-497_788-493delinsTCTGA ENSP00000420705.2:n.788-497_788-493delinsTCTGA
ENST00000493795.5:c.3861_3865delinsTCTGA ENSP00000418775.1:p.Gly1287=
ENST00000493919.5:c.647-497_647-493delinsTCTGA ENSP00000418819.1:n.647-497_647-493delinsTCTGA
ENST00000586385.5:c.5-27578_5-27574delinsTCTGA ENSP00000465818.1:n.5-27578_5-27574delinsTCTGA
ENST00000591534.5:c.-43-17008_-43-17004delinsTCTGA ENSP00000467329.1:n.-43-17008_-43-17004delinsTCTGA
ENST00000591849.5:c.-99+33742_-99+33746delinsTCTGA ENSP00000465347.1:n.-99+33742_-99+33746delinsTCTGA
NM_007294.3:c.4002_4006delinsTCTGA , LRG_292t1:c.4002_4006delinsTCTGA NP_009225.1:p.Gly1334=
NM_007297.3:c.3861_3865delinsTCTGA NP_009228.2:p.Gly1287=
NM_007298.3:c.788-497_788-493delinsTCTGA NP_009229.2:n.788-497_788-493delinsTCTGA
NM_007299.3:c.788-497_788-493delinsTCTGA NP_009230.2:n.788-497_788-493delinsTCTGA
NM_007300.3:c.4002_4006delinsTCTGA NP_009231.2:p.Gly1334=
NR_027676.1:n.4138_4142delinsTCTGA
NM_007294.4:c.4002_4006delinsTCTGA MANE Select NP_009225.1:p.Gly1334=
NM_007297.4:c.3861_3865delinsTCTGA NP_009228.2:p.Gly1287=
NM_007299.4:c.788-497_788-493delinsTCTGA NP_009230.2:n.788-497_788-493delinsTCTGA
NM_007300.4:c.4002_4006delinsTCTGA NP_009231.2:p.Gly1334=
NR_027676.2:n.4179_4183delinsTCTGA