Canonical Allele Identifier: CA2260782341
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43091835_43091836delinsAC , CM000679.2:g.43091835_43091836delinsAC GRCh38
NC_000017.10:g.41243852_41243853delinsAC , CM000679.1:g.41243852_41243853delinsAC GRCh37
NC_000017.9:g.38497378_38497379delinsAC NCBI36
NG_005905.2:g.126148_126149delinsGT , LRG_292:g.126148_126149delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.3759_3760delinsGT
ENST00000461574.2:c.3695_3696delinsGT ENSP00000417241.2:p.Gly1232=
ENST00000470026.6:c.3695_3696delinsGT ENSP00000419274.2:p.Gly1232=
ENST00000473961.6:c.3569_3570delinsGT ENSP00000420201.2:p.Gly1190=
ENST00000476777.6:c.3692_3693delinsGT ENSP00000417554.2:p.Gly1231=
ENST00000477152.6:c.3617_3618delinsGT ENSP00000419988.2:p.Gly1206=
ENST00000478531.6:c.785-804_785-803delinsGT ENSP00000420412.2:n.785-804_785-803delins...
ENST00000489037.2:c.3617_3618delinsGT ENSP00000420781.2:p.Gly1206=
ENST00000493919.6:c.647-804_647-803delinsGT ENSP00000418819.2:n.647-804_647-803delins...
ENST00000494123.6:c.3695_3696delinsGT ENSP00000419103.2:p.Gly1232=
ENST00000497488.2:c.2807_2808delinsGT ENSP00000418986.2:p.Gly936=
ENST00000618469.2:c.3695_3696delinsGT ENSP00000478114.2:p.Gly1232=
ENST00000634433.2:c.3572_3573delinsGT ENSP00000489431.2:p.Gly1191=
ENST00000644379.2:c.3695_3696delinsGT ENSP00000496570.2:p.Gly1232=
ENST00000644555.2:c.647-804_647-803delinsGT ENSP00000494614.2:n.647-804_647-803delins...
ENST00000652672.2:c.3554_3555delinsGT ENSP00000498906.2:p.Gly1185=
ENST00000484087.6:c.665-804_665-803delinsGT ENSP00000419481.2:n.665-804_665-803delins...
ENST00000700182.1:c.707-804_707-803delinsGT ENSP00000514849.1:n.707-804_707-803delins...
ENST00000357654.9:c.3695_3696delinsGT MANE Select ENSP00000350283.3:p.Gly1232=
ENST00000471181.7:c.3695_3696delinsGT ENSP00000418960.2:p.Gly1232=
ENST00000644379.1:c.16_17delinsGT
ENST00000352993.7:c.671-804_671-803delinsGT ENSP00000312236.5:n.671-804_671-803delins...
ENST00000354071.7:c.3695_3696delinsGT ENSP00000326002.7:p.Gly1232=
ENST00000357654.7:c.3695_3696delinsGT ENSP00000350283.3:p.Gly1232=
ENST00000461221.5:c.*3478_*3479delinsGT ENSP00000418548.1:n.*3478_*3479delinsGT
ENST00000468300.5:c.788-804_788-803delinsGT ENSP00000417148.1:n.788-804_788-803delins...
ENST00000471181.6:c.3695_3696delinsGT ENSP00000418960.2:p.Gly1232=
ENST00000478531.5:c.785-804_785-803delinsGT ENSP00000420412.1:n.785-804_785-803delins...
ENST00000484087.5:c.410-804_410-803delinsGT ENSP00000419481.1:n.410-804_410-803delins...
ENST00000487825.5:c.413-804_413-803delinsGT ENSP00000418212.1:n.413-804_413-803delins...
ENST00000491747.6:c.788-804_788-803delinsGT ENSP00000420705.2:n.788-804_788-803delins...
ENST00000493795.5:c.3554_3555delinsGT ENSP00000418775.1:p.Gly1185=
ENST00000493919.5:c.647-804_647-803delinsGT ENSP00000418819.1:n.647-804_647-803delins...
ENST00000586385.5:c.5-27885_5-27884delinsGT ENSP00000465818.1:n.5-27885_5-27884delins...
ENST00000591534.5:c.-43-17315_-43-17314delinsGT ENSP00000467329.1:n.-43-17315_-43-17314de...
ENST00000591849.5:c.-99+33435_-99+33436delinsGT ENSP00000465347.1:n.-99+33435_-99+33436de...
NM_007294.3:c.3695_3696delinsGT , LRG_292t1:c.3695_3696delinsGT NP_009225.1:p.Gly1232=
NM_007297.3:c.3554_3555delinsGT NP_009228.2:p.Gly1185=
NM_007298.3:c.788-804_788-803delinsGT NP_009229.2:n.788-804_788-803delinsGT
NM_007299.3:c.788-804_788-803delinsGT NP_009230.2:n.788-804_788-803delinsGT
NM_007300.3:c.3695_3696delinsGT NP_009231.2:p.Gly1232=
NR_027676.1:n.3831_3832delinsGT
NM_007294.4:c.3695_3696delinsGT MANE Select NP_009225.1:p.Gly1232=
NM_007297.4:c.3554_3555delinsGT NP_009228.2:p.Gly1185=
NM_007299.4:c.788-804_788-803delinsGT NP_009230.2:n.788-804_788-803delinsGT
NM_007300.4:c.3695_3696delinsGT NP_009231.2:p.Gly1232=
NR_027676.2:n.3872_3873delinsGT