Canonical Allele Identifier: CA772205911
Gene: BRCA1 HGNC NCBI

Linked Data

dbSNP Id: rs1223085865

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43099757_43099760del , CM000679.2:g.43099757_43099760del GRCh38
NC_000017.10:g.41251774_41251777del , CM000679.1:g.41251774_41251777del GRCh37
NC_000017.9:g.38505300_38505303del NCBI36
NG_005905.2:g.118226_118229del , LRG_292:g.118226_118229del

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.611+17_611+20del
ENST00000461574.2:c.547+17_547+20del ENSP00000417241.2:n.547+17_547+20del
ENST00000470026.6:c.547+17_547+20del ENSP00000419274.2:n.547+17_547+20del
ENST00000473961.6:c.544+17_544+20del ENSP00000420201.2:n.544+17_544+20del
ENST00000476777.6:c.544+17_544+20del ENSP00000417554.2:n.544+17_544+20del
ENST00000477152.6:c.469+17_469+20del ENSP00000419988.2:n.469+17_469+20del
ENST00000478531.6:c.544+17_544+20del ENSP00000420412.2:n.544+17_544+20del
ENST00000489037.2:c.469+17_469+20del ENSP00000420781.2:n.469+17_469+20del
ENST00000493919.6:c.406+17_406+20del ENSP00000418819.2:n.406+17_406+20del
ENST00000494123.6:c.547+17_547+20del ENSP00000419103.2:n.547+17_547+20del
ENST00000497488.2:c.-218-4898_-218-4895del ENSP00000418986.2:n.-218-4898_-218-4895del
ENST00000618469.2:c.547+17_547+20del ENSP00000478114.2:n.547+17_547+20del
ENST00000634433.2:c.547+17_547+20del ENSP00000489431.2:n.547+17_547+20del
ENST00000644379.2:c.547+17_547+20del ENSP00000496570.2:n.547+17_547+20del
ENST00000644555.2:c.406+17_406+20del ENSP00000494614.2:n.406+17_406+20del
ENST00000652672.2:c.406+17_406+20del ENSP00000498906.2:n.406+17_406+20del
ENST00000484087.6:c.547+17_547+20del ENSP00000419481.2:n.547+17_547+20del
ENST00000700182.1:c.466+17_466+20del ENSP00000514849.1:n.466+17_466+20del
ENST00000700183.1:c.*461+17_*461+20del ENSP00000514850.1:n.*461+17_*461+20del
ENST00000700184.1:n.804_807del
ENST00000357654.9:c.547+17_547+20del MANE Select ENSP00000350283.3:n.547+17_547+20del
ENST00000471181.7:c.547+17_547+20del ENSP00000418960.2:n.547+17_547+20del
ENST00000642945.1:c.*421+17_*421+20del ENSP00000495897.1:n.*421+17_*421+20del
ENST00000652672.1:c.406+17_406+20del ENSP00000498906.1:n.406+17_406+20del
ENST00000352993.7:c.547+17_547+20del ENSP00000312236.5:n.547+17_547+20del
ENST00000354071.7:c.547+17_547+20del ENSP00000326002.7:n.547+17_547+20del
ENST00000357654.7:c.547+17_547+20del ENSP00000350283.3:n.547+17_547+20del
ENST00000461221.5:c.*330+17_*330+20del ENSP00000418548.1:n.*330+17_*330+20del
ENST00000468300.5:c.547+17_547+20del ENSP00000417148.1:n.547+17_547+20del
ENST00000470026.5:c.547+17_547+20del ENSP00000419274.1:n.547+17_547+20del
ENST00000471181.6:c.547+17_547+20del ENSP00000418960.2:n.547+17_547+20del
ENST00000473961.5:c.267+17_267+20del
ENST00000476777.5:c.544+17_544+20del ENSP00000417554.1:n.544+17_544+20del
ENST00000477152.5:c.469+17_469+20del ENSP00000419988.1:n.469+17_469+20del
ENST00000478531.5:c.544+17_544+20del ENSP00000420412.1:n.544+17_544+20del
ENST00000484087.5:c.292+17_292+20del ENSP00000419481.1:n.292+17_292+20del
ENST00000487825.5:c.295+17_295+20del ENSP00000418212.1:n.295+17_295+20del
ENST00000491747.6:c.547+17_547+20del ENSP00000420705.2:n.547+17_547+20del
ENST00000492859.5:c.*483+17_*483+20del ENSP00000420253.1:n.*483+17_*483+20del
ENST00000493795.5:c.406+17_406+20del ENSP00000418775.1:n.406+17_406+20del
ENST00000493919.5:c.406+17_406+20del ENSP00000418819.1:n.406+17_406+20del
ENST00000494123.5:c.547+17_547+20del ENSP00000419103.1:n.547+17_547+20del
ENST00000497488.1:c.-218-4898_-218-4895del ENSP00000418986.1:n.-218-4898_-218-4895del
ENST00000586385.5:c.4+25424_4+25427del ENSP00000465818.1:n.4+25424_4+25427del
ENST00000591534.5:c.-43-25237_-43-25234del ENSP00000467329.1:n.-43-25237_-43-25234del
ENST00000591849.5:c.-99+25513_-99+25516del ENSP00000465347.1:n.-99+25513_-99+25516del
ENST00000634433.1:c.547+17_547+20del ENSP00000489431.1:n.547+17_547+20del
NM_007294.3:c.547+17_547+20del , LRG_292t1:c.547+17_547+20del NP_009225.1:n.547+17_547+20del
NM_007297.3:c.406+17_406+20del NP_009228.2:n.406+17_406+20del
NM_007298.3:c.547+17_547+20del NP_009229.2:n.547+17_547+20del
NM_007299.3:c.547+17_547+20del NP_009230.2:n.547+17_547+20del
NM_007300.3:c.547+17_547+20del NP_009231.2:n.547+17_547+20del
NR_027676.1:n.683+17_683+20del
NM_007294.4:c.547+17_547+20del MANE Select NP_009225.1:n.547+17_547+20del
NM_007297.4:c.406+17_406+20del NP_009228.2:n.406+17_406+20del
NM_007299.4:c.547+17_547+20del NP_009230.2:n.547+17_547+20del
NM_007300.4:c.547+17_547+20del NP_009231.2:n.547+17_547+20del
NR_027676.2:n.724+17_724+20del