Canonical Allele Identifier: CA002985
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 37608
dbSNP Id: rs80357887

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43099855_43099856del , CM000679.2:g.43099855_43099856del GRCh38
NC_000017.10:g.41251872_41251873del , CM000679.1:g.41251872_41251873del GRCh37
NC_000017.9:g.38505398_38505399del NCBI36
NG_005905.2:g.118132_118133del , LRG_292:g.118132_118133del

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.534_535del
ENST00000461574.2:c.470_471del ENSP00000417241.2:p.Ser157Ter
ENST00000470026.6:c.470_471del ENSP00000419274.2:p.Ser157Ter
ENST00000473961.6:c.467_468del ENSP00000420201.2:p.Ser156Ter
ENST00000476777.6:c.467_468del ENSP00000417554.2:p.Ser156Ter
ENST00000477152.6:c.392_393del ENSP00000419988.2:p.Ser131Ter
ENST00000478531.6:c.467_468del ENSP00000420412.2:p.Ser156Ter
ENST00000489037.2:c.392_393del ENSP00000420781.2:p.Ser131Ter
ENST00000493919.6:c.329_330del ENSP00000418819.2:p.Ser110Ter
ENST00000494123.6:c.470_471del ENSP00000419103.2:p.Ser157Ter
ENST00000497488.2:c.-218-4992_-218-4991del ENSP00000418986.2:n.-218-4992_-218-4991de...
ENST00000618469.2:c.470_471del ENSP00000478114.2:p.Ser157Ter
ENST00000634433.2:c.470_471del ENSP00000489431.2:p.Ser157Ter
ENST00000644379.2:c.470_471del ENSP00000496570.2:p.Ser157Ter
ENST00000644555.2:c.329_330del ENSP00000494614.2:p.Ser110Ter
ENST00000652672.2:c.329_330del ENSP00000498906.2:p.Ser110Ter
ENST00000484087.6:c.470_471del ENSP00000419481.2:p.Ser157Ter
ENST00000700182.1:c.389_390del ENSP00000514849.1:p.Ser130Ter
ENST00000700183.1:c.*384_*385del ENSP00000514850.1:n.*384_*385del
ENST00000700184.1:n.710_711del
ENST00000357654.9:c.470_471del MANE Select ENSP00000350283.3:p.Ser157Ter
ENST00000471181.7:c.470_471del ENSP00000418960.2:p.Ser157Ter
ENST00000642945.1:c.*344_*345del ENSP00000495897.1:n.*344_*345del
ENST00000652672.1:c.329_330del ENSP00000498906.1:p.Ser110Ter
ENST00000352993.7:c.470_471del ENSP00000312236.5:p.Ser157Ter
ENST00000354071.7:c.470_471del ENSP00000326002.7:p.Ser157Ter
ENST00000357654.7:c.470_471del ENSP00000350283.3:p.Ser157Ter
ENST00000461221.5:c.*253_*254del ENSP00000418548.1:n.*253_*254del
ENST00000461798.5:c.*256_*257del ENSP00000417988.1:n.*256_*257del
ENST00000468300.5:c.470_471del ENSP00000417148.1:p.Ser157Ter
ENST00000470026.5:c.470_471del ENSP00000419274.1:p.Ser157Ter
ENST00000471181.6:c.470_471del ENSP00000418960.2:p.Ser157Ter
ENST00000473961.5:c.190_191del
ENST00000476777.5:c.467_468del ENSP00000417554.1:p.Ser156Ter
ENST00000477152.5:c.392_393del ENSP00000419988.1:p.Ser131Ter
ENST00000478531.5:c.467_468del ENSP00000420412.1:p.Ser156Ter
ENST00000484087.5:c.215_216del ENSP00000419481.1:p.Ser72Ter
ENST00000487825.5:c.218_219del ENSP00000418212.1:p.Ser73Ter
ENST00000491747.6:c.470_471del ENSP00000420705.2:p.Ser157Ter
ENST00000492859.5:c.*406_*407del ENSP00000420253.1:n.*406_*407del
ENST00000493795.5:c.329_330del ENSP00000418775.1:p.Ser110Ter
ENST00000493919.5:c.329_330del ENSP00000418819.1:p.Ser110Ter
ENST00000494123.5:c.470_471del ENSP00000419103.1:p.Ser157Ter
ENST00000497488.1:c.-218-4992_-218-4991del ENSP00000418986.1:n.-218-4992_-218-4991de...
ENST00000586385.5:c.4+25330_4+25331del ENSP00000465818.1:n.4+25330_4+25331del
ENST00000591534.5:c.-43-25331_-43-25330del ENSP00000467329.1:n.-43-25331_-43-25330de...
ENST00000591849.5:c.-99+25419_-99+25420del ENSP00000465347.1:n.-99+25419_-99+25420de...
ENST00000634433.1:c.470_471del ENSP00000489431.1:p.Ser157Ter
NM_007294.3:c.470_471del , LRG_292t1:c.470_471del NP_009225.1:p.Ser157Ter
NM_007297.3:c.329_330del NP_009228.2:p.Ser110Ter
NM_007298.3:c.470_471del NP_009229.2:p.Ser157Ter
NM_007299.3:c.470_471del NP_009230.2:p.Ser157Ter
NM_007300.3:c.470_471del NP_009231.2:p.Ser157Ter
NR_027676.1:n.606_607del
NM_007294.4:c.470_471del MANE Select NP_009225.1:p.Ser157Ter
NM_007297.4:c.329_330del NP_009228.2:p.Ser110Ter
NM_007299.4:c.470_471del NP_009230.2:p.Ser157Ter
NM_007300.4:c.470_471del NP_009231.2:p.Ser157Ter
NR_027676.2:n.647_648del