Canonical Allele Identifier: CA919844506
Gene: BRCA1 HGNC NCBI

Linked Data

dbSNP Id: rs1567791324

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43092007_43092008insT , CM000679.2:g.43092007_43092008insT GRCh38
NC_000017.10:g.41244024_41244025insT , CM000679.1:g.41244024_41244025insT GRCh37
NC_000017.9:g.38497550_38497551insT NCBI36
NG_005905.2:g.125976_125977insA , LRG_292:g.125976_125977insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.3587_3588insA
ENST00000461574.2:c.3523_3524insA ENSP00000417241.2:p.Ala1175AspfsTer4
ENST00000470026.6:c.3523_3524insA ENSP00000419274.2:p.Ala1175AspfsTer4
ENST00000473961.6:c.3397_3398insA ENSP00000420201.2:p.Ala1133AspfsTer4
ENST00000476777.6:c.3520_3521insA ENSP00000417554.2:p.Ala1174AspfsTer4
ENST00000477152.6:c.3445_3446insA ENSP00000419988.2:p.Ala1149AspfsTer4
ENST00000478531.6:c.785-976_785-975insA ENSP00000420412.2:n.785-976_785-975insA
ENST00000489037.2:c.3445_3446insA ENSP00000420781.2:p.Ala1149AspfsTer4
ENST00000493919.6:c.647-976_647-975insA ENSP00000418819.2:n.647-976_647-975insA
ENST00000494123.6:c.3523_3524insA ENSP00000419103.2:p.Ala1175AspfsTer4
ENST00000497488.2:c.2635_2636insA ENSP00000418986.2:p.Ala879AspfsTer4
ENST00000618469.2:c.3523_3524insA ENSP00000478114.2:p.Ala1175AspfsTer4
ENST00000634433.2:c.3400_3401insA ENSP00000489431.2:p.Ala1134AspfsTer4
ENST00000644379.2:c.3523_3524insA ENSP00000496570.2:p.Ala1175AspfsTer4
ENST00000644555.2:c.647-976_647-975insA ENSP00000494614.2:n.647-976_647-975insA
ENST00000652672.2:c.3382_3383insA ENSP00000498906.2:p.Ala1128AspfsTer4
ENST00000484087.6:c.665-976_665-975insA ENSP00000419481.2:n.665-976_665-975insA
ENST00000700182.1:c.707-976_707-975insA ENSP00000514849.1:n.707-976_707-975insA
ENST00000357654.9:c.3523_3524insA MANE Select ENSP00000350283.3:p.Ala1175AspfsTer4
ENST00000471181.7:c.3523_3524insA ENSP00000418960.2:p.Ala1175AspfsTer4
ENST00000352993.7:c.671-976_671-975insA ENSP00000312236.5:n.671-976_671-975insA
ENST00000354071.7:c.3523_3524insA ENSP00000326002.7:p.Ala1175AspfsTer4
ENST00000357654.7:c.3523_3524insA ENSP00000350283.3:p.Ala1175AspfsTer4
ENST00000461221.5:c.*3306_*3307insA ENSP00000418548.1:n.*3306_*3307insA
ENST00000468300.5:c.788-976_788-975insA ENSP00000417148.1:n.788-976_788-975insA
ENST00000471181.6:c.3523_3524insA ENSP00000418960.2:p.Ala1175AspfsTer4
ENST00000478531.5:c.785-976_785-975insA ENSP00000420412.1:n.785-976_785-975insA
ENST00000484087.5:c.410-976_410-975insA ENSP00000419481.1:n.410-976_410-975insA
ENST00000487825.5:c.413-976_413-975insA ENSP00000418212.1:n.413-976_413-975insA
ENST00000491747.6:c.788-976_788-975insA ENSP00000420705.2:n.788-976_788-975insA
ENST00000493795.5:c.3382_3383insA ENSP00000418775.1:p.Ala1128AspfsTer4
ENST00000493919.5:c.647-976_647-975insA ENSP00000418819.1:n.647-976_647-975insA
ENST00000586385.5:c.5-28057_5-28056insA ENSP00000465818.1:n.5-28057_5-28056insA
ENST00000591534.5:c.-43-17487_-43-17486insA ENSP00000467329.1:n.-43-17487_-43-17486insA
ENST00000591849.5:c.-99+33263_-99+33264insA ENSP00000465347.1:n.-99+33263_-99+33264insA
NM_007294.3:c.3523_3524insA , LRG_292t1:c.3523_3524insA NP_009225.1:p.Ala1175AspfsTer4
NM_007297.3:c.3382_3383insA NP_009228.2:p.Ala1128AspfsTer4
NM_007298.3:c.788-976_788-975insA NP_009229.2:n.788-976_788-975insA
NM_007299.3:c.788-976_788-975insA NP_009230.2:n.788-976_788-975insA
NM_007300.3:c.3523_3524insA NP_009231.2:p.Ala1175AspfsTer4
NR_027676.1:n.3659_3660insA
NM_007294.4:c.3523_3524insA MANE Select NP_009225.1:p.Ala1175AspfsTer4
NM_007297.4:c.3382_3383insA NP_009228.2:p.Ala1128AspfsTer4
NM_007299.4:c.788-976_788-975insA NP_009230.2:n.788-976_788-975insA
NM_007300.4:c.3523_3524insA NP_009231.2:p.Ala1175AspfsTer4
NR_027676.2:n.3700_3701insA