Canonical Allele Identifier: CA2809538984
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43092008_43092009del , CM000679.2:g.43092008_43092009del GRCh38
NC_000017.10:g.41244025_41244026del , CM000679.1:g.41244025_41244026del GRCh37
NC_000017.9:g.38497551_38497552del NCBI36
NG_005905.2:g.125975_125976del , LRG_292:g.125975_125976del

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.3586_3587del
ENST00000461574.2:c.3522_3523del ENSP00000417241.2:p.Ala1175CysfsTer3
ENST00000470026.6:c.3522_3523del ENSP00000419274.2:p.Ala1175CysfsTer3
ENST00000473961.6:c.3396_3397del ENSP00000420201.2:p.Ala1133CysfsTer3
ENST00000476777.6:c.3519_3520del ENSP00000417554.2:p.Ala1174CysfsTer3
ENST00000477152.6:c.3444_3445del ENSP00000419988.2:p.Ala1149CysfsTer3
ENST00000478531.6:c.785-977_785-976del ENSP00000420412.2:n.785-977_785-976del
ENST00000489037.2:c.3444_3445del ENSP00000420781.2:p.Ala1149CysfsTer3
ENST00000493919.6:c.647-977_647-976del ENSP00000418819.2:n.647-977_647-976del
ENST00000494123.6:c.3522_3523del ENSP00000419103.2:p.Ala1175CysfsTer3
ENST00000497488.2:c.2634_2635del ENSP00000418986.2:p.Ala879CysfsTer3
ENST00000618469.2:c.3522_3523del ENSP00000478114.2:p.Ala1175CysfsTer3
ENST00000634433.2:c.3399_3400del ENSP00000489431.2:p.Ala1134CysfsTer3
ENST00000644379.2:c.3522_3523del ENSP00000496570.2:p.Ala1175CysfsTer3
ENST00000644555.2:c.647-977_647-976del ENSP00000494614.2:n.647-977_647-976del
ENST00000652672.2:c.3381_3382del ENSP00000498906.2:p.Ala1128CysfsTer3
ENST00000484087.6:c.665-977_665-976del ENSP00000419481.2:n.665-977_665-976del
ENST00000700182.1:c.707-977_707-976del ENSP00000514849.1:n.707-977_707-976del
ENST00000357654.9:c.3522_3523del MANE Select ENSP00000350283.3:p.Ala1175CysfsTer3
ENST00000471181.7:c.3522_3523del ENSP00000418960.2:p.Ala1175CysfsTer3
ENST00000352993.7:c.671-977_671-976del ENSP00000312236.5:n.671-977_671-976del
ENST00000354071.7:c.3522_3523del ENSP00000326002.7:p.Ala1175CysfsTer3
ENST00000357654.7:c.3522_3523del ENSP00000350283.3:p.Ala1175CysfsTer3
ENST00000461221.5:c.*3305_*3306del ENSP00000418548.1:n.*3305_*3306del
ENST00000468300.5:c.788-977_788-976del ENSP00000417148.1:n.788-977_788-976del
ENST00000471181.6:c.3522_3523del ENSP00000418960.2:p.Ala1175CysfsTer3
ENST00000478531.5:c.785-977_785-976del ENSP00000420412.1:n.785-977_785-976del
ENST00000484087.5:c.410-977_410-976del ENSP00000419481.1:n.410-977_410-976del
ENST00000487825.5:c.413-977_413-976del ENSP00000418212.1:n.413-977_413-976del
ENST00000491747.6:c.788-977_788-976del ENSP00000420705.2:n.788-977_788-976del
ENST00000493795.5:c.3381_3382del ENSP00000418775.1:p.Ala1128CysfsTer3
ENST00000493919.5:c.647-977_647-976del ENSP00000418819.1:n.647-977_647-976del
ENST00000586385.5:c.5-28058_5-28057del ENSP00000465818.1:n.5-28058_5-28057del
ENST00000591534.5:c.-43-17488_-43-17487del ENSP00000467329.1:n.-43-17488_-43-17487del
ENST00000591849.5:c.-99+33262_-99+33263del ENSP00000465347.1:n.-99+33262_-99+33263del
NM_007294.3:c.3522_3523del , LRG_292t1:c.3522_3523del NP_009225.1:p.Ala1175CysfsTer3
NM_007297.3:c.3381_3382del NP_009228.2:p.Ala1128CysfsTer3
NM_007298.3:c.788-977_788-976del NP_009229.2:n.788-977_788-976del
NM_007299.3:c.788-977_788-976del NP_009230.2:n.788-977_788-976del
NM_007300.3:c.3522_3523del NP_009231.2:p.Ala1175CysfsTer3
NR_027676.1:n.3658_3659del
NM_007294.4:c.3522_3523del MANE Select NP_009225.1:p.Ala1175CysfsTer3
NM_007297.4:c.3381_3382del NP_009228.2:p.Ala1128CysfsTer3
NM_007299.4:c.788-977_788-976del NP_009230.2:n.788-977_788-976del
NM_007300.4:c.3522_3523del NP_009231.2:p.Ala1175CysfsTer3
NR_027676.2:n.3699_3700del