Canonical Allele Identifier: CA16043341
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 373823
ClinVar RCV Id: RCV001390964
dbSNP Id: rs1057518636

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43047646_43047647insA , CM000679.2:g.43047646_43047647insA GRCh38
NC_000017.10:g.41199663_41199664insA , CM000679.1:g.41199663_41199664insA GRCh37
NC_000017.9:g.38453189_38453190insA NCBI36
NG_005905.2:g.170337_170338insT , LRG_292:g.170337_170338insT

Transcript Alleles

HGVS Amino-acid change
ENST00000461574.2:c.5460_5461insT ENSP00000417241.2:p.His1821SerfsTer8
ENST00000470026.6:c.5463_5464insT ENSP00000419274.2:p.His1822SerfsTer8
ENST00000473961.6:c.5337_5338insT ENSP00000420201.2:p.His1780SerfsTer8
ENST00000476777.6:c.5457_5458insT ENSP00000417554.2:p.His1820SerfsTer8
ENST00000477152.6:c.5385_5386insT ENSP00000419988.2:p.His1796SerfsTer8
ENST00000478531.6:c.2151_2152insT ENSP00000420412.2:p.His718SerfsTer8
ENST00000489037.2:c.5385_5386insT ENSP00000420781.2:p.His1796SerfsTer8
ENST00000493919.6:c.2013_2014insT ENSP00000418819.2:p.His672SerfsTer8
ENST00000494123.6:c.5463_5464insT ENSP00000419103.2:p.His1822SerfsTer8
ENST00000497488.2:c.4575_4576insT ENSP00000418986.2:p.His1526SerfsTer8
ENST00000618469.2:c.5463_5464insT ENSP00000478114.2:p.His1822SerfsTer8
ENST00000634433.2:c.5340_5341insT ENSP00000489431.2:p.His1781SerfsTer8
ENST00000644379.2:c.5529_5530insT ENSP00000496570.2:p.His1844SerfsTer8
ENST00000644555.2:c.2013_2014insT ENSP00000494614.2:p.His672SerfsTer8
ENST00000652672.2:c.5322_5323insT ENSP00000498906.2:p.His1775SerfsTer8
ENST00000484087.6:c.2025_2026insT ENSP00000419481.2:p.His676SerfsTer8
ENST00000700081.1:n.1346_1347insT
ENST00000700082.1:n.827_828insT
ENST00000357654.9:c.5463_5464insT MANE Select ENSP00000350283.3:p.His1822SerfsTer8
ENST00000471181.7:c.5526_5527insT ENSP00000418960.2:p.His1843SerfsTer8
ENST00000644379.1:c.1850_1851insT
ENST00000352993.7:c.2037_2038insT ENSP00000312236.5:p.His680SerfsTer8
ENST00000357654.7:c.5463_5464insT ENSP00000350283.3:p.His1822SerfsTer8
ENST00000461221.5:c.*5246_*5247insT ENSP00000418548.1:n.*5246_*5247insT
ENST00000468300.5:c.2077_2078insT ENSP00000417148.1:p.Pro693LeufsTer13
ENST00000471181.6:c.5526_5527insT ENSP00000418960.2:p.His1843SerfsTer8
ENST00000491747.6:c.2151_2152insT ENSP00000420705.2:p.His718SerfsTer8
ENST00000493795.5:c.5322_5323insT ENSP00000418775.1:p.His1775SerfsTer8
ENST00000586385.5:c.393_394insT ENSP00000465818.1:p.His132SerfsTer8
ENST00000591534.5:c.936_937insT ENSP00000467329.1:p.His313SerfsTer8
ENST00000591849.5:c.162_163insT ENSP00000465347.1:p.His55SerfsTer8
NM_007294.3:c.5463_5464insT , LRG_292t1:c.5463_5464insT NP_009225.1:p.His1822SerfsTer8
NM_007297.3:c.5322_5323insT NP_009228.2:p.His1775SerfsTer8
NM_007298.3:c.2151_2152insT NP_009229.2:p.His718SerfsTer8
NM_007299.3:c.2077_2078insT NP_009230.2:p.Pro693LeufsTer13
NM_007300.3:c.5526_5527insT NP_009231.2:p.His1843SerfsTer8
NR_027676.1:n.5599_5600insT
NM_007294.4:c.5463_5464insT MANE Select NP_009225.1:p.His1822SerfsTer8
NM_007297.4:c.5322_5323insT NP_009228.2:p.His1775SerfsTer8
NM_007299.4:c.2077_2078insT NP_009230.2:p.Pro693LeufsTer13
NM_007300.4:c.5526_5527insT NP_009231.2:p.His1843SerfsTer8
NR_027676.2:n.5640_5641insT