Canonical Allele Identifier: CA919844194
Gene: BRCA1 HGNC NCBI

Linked Data

dbSNP Id: rs1567774796

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43071028del , CM000679.2:g.43071028del GRCh38
NC_000017.10:g.41223045del , CM000679.1:g.41223045del GRCh37
NC_000017.9:g.38476571del NCBI36
NG_005905.2:g.146957del , LRG_292:g.146957del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.4884del ENSP00000417241.2:p.Glu1629LysfsTer3
ENST00000470026.6:c.4887del ENSP00000419274.2:p.Glu1630LysfsTer3
ENST00000473961.6:c.4761del ENSP00000420201.2:p.Glu1588LysfsTer3
ENST00000476777.6:c.4881del ENSP00000417554.2:p.Glu1628LysfsTer3
ENST00000477152.6:c.4809del ENSP00000419988.2:p.Glu1604LysfsTer3
ENST00000478531.6:c.1575del ENSP00000420412.2:p.Glu526LysfsTer3
ENST00000489037.2:c.4809del ENSP00000420781.2:p.Glu1604LysfsTer3
ENST00000493919.6:c.1437del ENSP00000418819.2:p.Glu480LysfsTer3
ENST00000494123.6:c.4887del ENSP00000419103.2:p.Glu1630LysfsTer3
ENST00000497488.2:c.3999del ENSP00000418986.2:p.Glu1334LysfsTer3
ENST00000618469.2:c.4887del ENSP00000478114.2:p.Glu1630LysfsTer3
ENST00000634433.2:c.4764del ENSP00000489431.2:p.Glu1589LysfsTer3
ENST00000644379.2:c.4953del ENSP00000496570.2:p.Glu1652LysfsTer3
ENST00000644555.2:c.1437del ENSP00000494614.2:p.Glu480LysfsTer3
ENST00000652672.2:c.4746del ENSP00000498906.2:p.Glu1583LysfsTer3
ENST00000484087.6:c.1449del ENSP00000419481.2:p.Glu484LysfsTer3
ENST00000700182.1:c.1494del ENSP00000514849.1:p.Glu499LysfsTer3
ENST00000357654.9:c.4887del MANE Select ENSP00000350283.3:p.Glu1630LysfsTer3
ENST00000471181.7:c.4950del ENSP00000418960.2:p.Glu1651LysfsTer3
ENST00000644379.1:c.1274del
ENST00000352993.7:c.1461del ENSP00000312236.5:p.Glu488LysfsTer3
ENST00000357654.7:c.4887del ENSP00000350283.3:p.Glu1630LysfsTer3
ENST00000461221.5:c.*4670del ENSP00000418548.1:n.*4670del
ENST00000468300.5:c.1575del ENSP00000417148.1:p.Glu526LysfsTer3
ENST00000471181.6:c.4950del ENSP00000418960.2:p.Glu1651LysfsTer3
ENST00000472490.1:n.40del
ENST00000478531.5:c.1575del ENSP00000420412.1:p.Glu526LysfsTer3
ENST00000484087.5:c.1200del ENSP00000419481.1:p.Glu401LysfsTer3
ENST00000491747.6:c.1575del ENSP00000420705.2:p.Glu526LysfsTer3
ENST00000493795.5:c.4746del ENSP00000418775.1:p.Glu1583LysfsTer3
ENST00000493919.5:c.1437del ENSP00000418819.1:p.Glu480LysfsTer3
ENST00000586385.5:c.5-7076del ENSP00000465818.1:n.5-7076del
ENST00000591534.5:c.360del ENSP00000467329.1:p.Glu121LysfsTer3
ENST00000591849.5:c.-98-20837del ENSP00000465347.1:n.-98-20837del
NM_007294.3:c.4887del , LRG_292t1:c.4887del NP_009225.1:p.Glu1630LysfsTer3
NM_007297.3:c.4746del NP_009228.2:p.Glu1583LysfsTer3
NM_007298.3:c.1575del NP_009229.2:p.Glu526LysfsTer3
NM_007299.3:c.1575del NP_009230.2:p.Glu526LysfsTer3
NM_007300.3:c.4950del NP_009231.2:p.Glu1651LysfsTer3
NR_027676.1:n.5023del
NM_007294.4:c.4887del MANE Select NP_009225.1:p.Glu1630LysfsTer3
NM_007297.4:c.4746del NP_009228.2:p.Glu1583LysfsTer3
NM_007299.4:c.1575del NP_009230.2:p.Glu526LysfsTer3
NM_007300.4:c.4950del NP_009231.2:p.Glu1651LysfsTer3
NR_027676.2:n.5064del