Canonical Allele Identifier: CA2260781981
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43091496_43091499delinsTTCA , CM000679.2:g.43091496_43091499delinsTTCA GRCh38
NC_000017.10:g.41243513_41243516delinsTTCA , CM000679.1:g.41243513_41243516delinsTTCA GRCh37
NC_000017.9:g.38497039_38497042delinsTTCA NCBI36
NG_005905.2:g.126485_126488delinsTGAA , LRG_292:g.126485_126488delinsTGAA

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.4096_4099delinsTGAA
ENST00000461574.2:c.4032_4035delinsTGAA ENSP00000417241.2:p.Asp1344=
ENST00000470026.6:c.4032_4035delinsTGAA ENSP00000419274.2:p.Asp1344=
ENST00000473961.6:c.3906_3909delinsTGAA ENSP00000420201.2:p.Asp1302=
ENST00000476777.6:c.4029_4032delinsTGAA ENSP00000417554.2:p.Asp1343=
ENST00000477152.6:c.3954_3957delinsTGAA ENSP00000419988.2:p.Asp1318=
ENST00000478531.6:c.785-467_785-464delinsTGAA ENSP00000420412.2:n.785-467_785-464delins...
ENST00000489037.2:c.3954_3957delinsTGAA ENSP00000420781.2:p.Asp1318=
ENST00000493919.6:c.647-467_647-464delinsTGAA ENSP00000418819.2:n.647-467_647-464delins...
ENST00000494123.6:c.4032_4035delinsTGAA ENSP00000419103.2:p.Asp1344=
ENST00000497488.2:c.3144_3147delinsTGAA ENSP00000418986.2:p.Asp1048=
ENST00000618469.2:c.4032_4035delinsTGAA ENSP00000478114.2:p.Asp1344=
ENST00000634433.2:c.3909_3912delinsTGAA ENSP00000489431.2:p.Asp1303=
ENST00000644379.2:c.4032_4035delinsTGAA ENSP00000496570.2:p.Asp1344=
ENST00000644555.2:c.647-467_647-464delinsTGAA ENSP00000494614.2:n.647-467_647-464delins...
ENST00000652672.2:c.3891_3894delinsTGAA ENSP00000498906.2:p.Asp1297=
ENST00000484087.6:c.665-467_665-464delinsTGAA ENSP00000419481.2:n.665-467_665-464delins...
ENST00000700182.1:c.707-467_707-464delinsTGAA ENSP00000514849.1:n.707-467_707-464delins...
ENST00000357654.9:c.4032_4035delinsTGAA MANE Select ENSP00000350283.3:p.Asp1344=
ENST00000471181.7:c.4032_4035delinsTGAA ENSP00000418960.2:p.Asp1344=
ENST00000644379.1:c.353_356delinsTGAA
ENST00000352993.7:c.671-467_671-464delinsTGAA ENSP00000312236.5:n.671-467_671-464delins...
ENST00000354071.7:c.4032_4035delinsTGAA ENSP00000326002.7:p.Asp1344=
ENST00000357654.7:c.4032_4035delinsTGAA ENSP00000350283.3:p.Asp1344=
ENST00000461221.5:c.*3815_*3818delinsTGAA ENSP00000418548.1:n.*3815_*3818delinsTGAA...
ENST00000461574.1:c.326_329delinsTGAA
ENST00000468300.5:c.788-467_788-464delinsTGAA ENSP00000417148.1:n.788-467_788-464delins...
ENST00000471181.6:c.4032_4035delinsTGAA ENSP00000418960.2:p.Asp1344=
ENST00000478531.5:c.785-467_785-464delinsTGAA ENSP00000420412.1:n.785-467_785-464delins...
ENST00000484087.5:c.410-467_410-464delinsTGAA ENSP00000419481.1:n.410-467_410-464delins...
ENST00000487825.5:c.413-467_413-464delinsTGAA ENSP00000418212.1:n.413-467_413-464delins...
ENST00000491747.6:c.788-467_788-464delinsTGAA ENSP00000420705.2:n.788-467_788-464delins...
ENST00000493795.5:c.3891_3894delinsTGAA ENSP00000418775.1:p.Asp1297=
ENST00000493919.5:c.647-467_647-464delinsTGAA ENSP00000418819.1:n.647-467_647-464delins...
ENST00000586385.5:c.5-27548_5-27545delinsTGAA ENSP00000465818.1:n.5-27548_5-27545delins...
ENST00000591534.5:c.-43-16978_-43-16975delinsTGAA ENSP00000467329.1:n.-43-16978_-43-16975de...
ENST00000591849.5:c.-99+33772_-99+33775delinsTGAA ENSP00000465347.1:n.-99+33772_-99+33775de...
NM_007294.3:c.4032_4035delinsTGAA , LRG_292t1:c.4032_4035delinsTGAA NP_009225.1:p.Asp1344=
NM_007297.3:c.3891_3894delinsTGAA NP_009228.2:p.Asp1297=
NM_007298.3:c.788-467_788-464delinsTGAA NP_009229.2:n.788-467_788-464delinsTGAA
NM_007299.3:c.788-467_788-464delinsTGAA NP_009230.2:n.788-467_788-464delinsTGAA
NM_007300.3:c.4032_4035delinsTGAA NP_009231.2:p.Asp1344=
NR_027676.1:n.4168_4171delinsTGAA
NM_007294.4:c.4032_4035delinsTGAA MANE Select NP_009225.1:p.Asp1344=
NM_007297.4:c.3891_3894delinsTGAA NP_009228.2:p.Asp1297=
NM_007299.4:c.788-467_788-464delinsTGAA NP_009230.2:n.788-467_788-464delinsTGAA
NM_007300.4:c.4032_4035delinsTGAA NP_009231.2:p.Asp1344=
NR_027676.2:n.4209_4212delinsTGAA