Canonical Allele Identifier: CA2260777951
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43082404_43082405delinsCT , CM000679.2:g.43082404_43082405delinsCT GRCh38
NC_000017.10:g.41234421_41234422delinsCT , CM000679.1:g.41234421_41234422delinsCT GRCh37
NC_000017.9:g.38487947_38487948delinsCT NCBI36
NG_005905.2:g.135579_135580delinsAG , LRG_292:g.135579_135580delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.4356_4357delinsAG ENSP00000417241.2:p.Lys1452=
ENST00000470026.6:c.4356_4357delinsAG ENSP00000419274.2:p.Lys1452=
ENST00000473961.6:c.4230_4231delinsAG ENSP00000420201.2:p.Lys1410=
ENST00000476777.6:c.4350_4351delinsAG ENSP00000417554.2:p.Lys1450=
ENST00000477152.6:c.4278_4279delinsAG ENSP00000419988.2:p.Lys1426=
ENST00000478531.6:c.1044_1045delinsAG ENSP00000420412.2:p.Lys348=
ENST00000489037.2:c.4278_4279delinsAG ENSP00000420781.2:p.Lys1426=
ENST00000493919.6:c.906_907delinsAG ENSP00000418819.2:p.Lys302=
ENST00000494123.6:c.4356_4357delinsAG ENSP00000419103.2:p.Lys1452=
ENST00000497488.2:c.3468_3469delinsAG ENSP00000418986.2:p.Lys1156=
ENST00000618469.2:c.4356_4357delinsAG ENSP00000478114.2:p.Lys1452=
ENST00000634433.2:c.4233_4234delinsAG ENSP00000489431.2:p.Lys1411=
ENST00000644379.2:c.4356_4357delinsAG ENSP00000496570.2:p.Lys1452=
ENST00000644555.2:c.906_907delinsAG ENSP00000494614.2:p.Lys302=
ENST00000652672.2:c.4215_4216delinsAG ENSP00000498906.2:p.Lys1405=
ENST00000484087.6:c.921_922delinsAG ENSP00000419481.2:p.Lys307=
ENST00000700182.1:c.966_967delinsAG ENSP00000514849.1:p.Lys322=
ENST00000357654.9:c.4356_4357delinsAG MANE Select ENSP00000350283.3:p.Lys1452=
ENST00000471181.7:c.4356_4357delinsAG ENSP00000418960.2:p.Lys1452=
ENST00000644379.1:c.677_678delinsAG
ENST00000352993.7:c.930_931delinsAG ENSP00000312236.5:p.Lys310=
ENST00000357654.7:c.4356_4357delinsAG ENSP00000350283.3:p.Lys1452=
ENST00000461221.5:c.*4139_*4140delinsAG ENSP00000418548.1:n.*4139_*4140delinsAG
ENST00000461574.1:c.650_651delinsAG
ENST00000468300.5:c.1047_1048delinsAG ENSP00000417148.1:p.Lys349=
ENST00000471181.6:c.4356_4357delinsAG ENSP00000418960.2:p.Lys1452=
ENST00000478531.5:c.1044_1045delinsAG ENSP00000420412.1:p.Lys348=
ENST00000484087.5:c.669_670delinsAG ENSP00000419481.1:p.Lys223=
ENST00000487825.5:c.672_673delinsAG ENSP00000418212.1:p.Lys224=
ENST00000491747.6:c.1047_1048delinsAG ENSP00000420705.2:p.Lys349=
ENST00000493795.5:c.4215_4216delinsAG ENSP00000418775.1:p.Lys1405=
ENST00000493919.5:c.906_907delinsAG ENSP00000418819.1:p.Lys302=
ENST00000586385.5:c.5-18454_5-18453delinsAG ENSP00000465818.1:n.5-18454_5-18453delinsAG
ENST00000591534.5:c.-43-7884_-43-7883delinsAG ENSP00000467329.1:n.-43-7884_-43-7883delinsAG
ENST00000591849.5:c.-98-32215_-98-32214delinsAG ENSP00000465347.1:n.-98-32215_-98-32214delinsAG
ENST00000621897.1:n.250_251delinsAG
NM_007294.3:c.4356_4357delinsAG , LRG_292t1:c.4356_4357delinsAG NP_009225.1:p.Lys1452=
NM_007297.3:c.4215_4216delinsAG NP_009228.2:p.Lys1405=
NM_007298.3:c.1047_1048delinsAG NP_009229.2:p.Lys349=
NM_007299.3:c.1047_1048delinsAG NP_009230.2:p.Lys349=
NM_007300.3:c.4356_4357delinsAG NP_009231.2:p.Lys1452=
NR_027676.1:n.4492_4493delinsAG
NM_007294.4:c.4356_4357delinsAG MANE Select NP_009225.1:p.Lys1452=
NM_007297.4:c.4215_4216delinsAG NP_009228.2:p.Lys1405=
NM_007299.4:c.1047_1048delinsAG NP_009230.2:p.Lys349=
NM_007300.4:c.4356_4357delinsAG NP_009231.2:p.Lys1452=
NR_027676.2:n.4533_4534delinsAG