Canonical Allele Identifier: CA10585909
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 252399
dbSNP Id: rs879255295

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43070941del , CM000679.2:g.43070941del GRCh38
NC_000017.10:g.41222958del , CM000679.1:g.41222958del GRCh37
NC_000017.9:g.38476484del NCBI36
NG_005905.2:g.147046del , LRG_292:g.147046del

Transcript Alleles

HGVS Amino-acid change
ENST00000461574.2:c.4973del ENSP00000417241.2:p.Pro1658GlnfsTer18
ENST00000470026.6:c.4976del ENSP00000419274.2:p.Pro1659GlnfsTer18
ENST00000473961.6:c.4850del ENSP00000420201.2:p.Pro1617GlnfsTer18
ENST00000476777.6:c.4970del ENSP00000417554.2:p.Pro1657GlnfsTer18
ENST00000477152.6:c.4898del ENSP00000419988.2:p.Pro1633GlnfsTer18
ENST00000478531.6:c.1664del ENSP00000420412.2:p.Pro555GlnfsTer18
ENST00000489037.2:c.4898del ENSP00000420781.2:p.Pro1633GlnfsTer18
ENST00000493919.6:c.1526del ENSP00000418819.2:p.Pro509GlnfsTer18
ENST00000494123.6:c.4976del ENSP00000419103.2:p.Pro1659GlnfsTer18
ENST00000497488.2:c.4088del ENSP00000418986.2:p.Pro1363GlnfsTer18
ENST00000618469.2:c.4976del ENSP00000478114.2:p.Pro1659GlnfsTer18
ENST00000634433.2:c.4853del ENSP00000489431.2:p.Pro1618GlnfsTer18
ENST00000644379.2:c.5042del ENSP00000496570.2:p.Pro1681GlnfsTer18
ENST00000644555.2:c.1526del ENSP00000494614.2:p.Pro509GlnfsTer18
ENST00000652672.2:c.4835del ENSP00000498906.2:p.Pro1612GlnfsTer18
ENST00000484087.6:c.1538del ENSP00000419481.2:p.Pro513GlnfsTer18
ENST00000700182.1:c.1583del ENSP00000514849.1:p.Pro528GlnfsTer5
ENST00000357654.9:c.4976del MANE Select ENSP00000350283.3:p.Pro1659GlnfsTer18
ENST00000471181.7:c.5039del ENSP00000418960.2:p.Pro1680GlnfsTer18
ENST00000644379.1:c.1363del
ENST00000352993.7:c.1550del ENSP00000312236.5:p.Pro517GlnfsTer18
ENST00000357654.7:c.4976del ENSP00000350283.3:p.Pro1659GlnfsTer18
ENST00000461221.5:c.*4759del ENSP00000418548.1:n.*4759del
ENST00000468300.5:c.1664del ENSP00000417148.1:p.Pro555GlnfsTer18
ENST00000471181.6:c.5039del ENSP00000418960.2:p.Pro1680GlnfsTer18
ENST00000472490.1:n.129del
ENST00000478531.5:c.1664del ENSP00000420412.1:p.Pro555GlnfsTer18
ENST00000484087.5:c.1289del ENSP00000419481.1:p.Pro430GlnfsTer18
ENST00000491747.6:c.1664del ENSP00000420705.2:p.Pro555GlnfsTer18
ENST00000493795.5:c.4835del ENSP00000418775.1:p.Pro1612GlnfsTer18
ENST00000493919.5:c.1526del ENSP00000418819.1:p.Pro509GlnfsTer18
ENST00000586385.5:c.5-6987del ENSP00000465818.1:n.5-6987del
ENST00000591534.5:c.449del ENSP00000467329.1:p.Pro150GlnfsTer18
ENST00000591849.5:c.-98-20748del ENSP00000465347.1:n.-98-20748del
NM_007294.3:c.4976del , LRG_292t1:c.4976del NP_009225.1:p.Pro1659GlnfsTer18
NM_007297.3:c.4835del NP_009228.2:p.Pro1612GlnfsTer18
NM_007298.3:c.1664del NP_009229.2:p.Pro555GlnfsTer18
NM_007299.3:c.1664del NP_009230.2:p.Pro555GlnfsTer18
NM_007300.3:c.5039del NP_009231.2:p.Pro1680GlnfsTer18
NR_027676.1:n.5112del
NM_007294.4:c.4976del MANE Select NP_009225.1:p.Pro1659GlnfsTer18
NM_007297.4:c.4835del NP_009228.2:p.Pro1612GlnfsTer18
NM_007299.4:c.1664del NP_009230.2:p.Pro555GlnfsTer18
NM_007300.4:c.5039del NP_009231.2:p.Pro1680GlnfsTer18
NR_027676.2:n.5153del