Canonical Allele Identifier: CA2260782087
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43091605T= , CM000679.2:g.43091605T= GRCh38
NC_000017.10:g.41243622T= , CM000679.1:g.41243622T= GRCh37
NC_000017.9:g.38497148T= NCBI36
NG_005905.2:g.126379A= , LRG_292:g.126379A=

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.3990A=
ENST00000461574.2:c.3926A= ENSP00000417241.2:p.Asn1309=
ENST00000470026.6:c.3926A= ENSP00000419274.2:p.Asn1309=
ENST00000473961.6:c.3800A= ENSP00000420201.2:p.Asn1267=
ENST00000476777.6:c.3923A= ENSP00000417554.2:p.Asn1308=
ENST00000477152.6:c.3848A= ENSP00000419988.2:p.Asn1283=
ENST00000478531.6:c.785-573A= ENSP00000420412.2:n.785-573A=
ENST00000489037.2:c.3848A= ENSP00000420781.2:p.Asn1283=
ENST00000493919.6:c.647-573A= ENSP00000418819.2:n.647-573A=
ENST00000494123.6:c.3926A= ENSP00000419103.2:p.Asn1309=
ENST00000497488.2:c.3038A= ENSP00000418986.2:p.Asn1013=
ENST00000618469.2:c.3926A= ENSP00000478114.2:p.Asn1309=
ENST00000634433.2:c.3803A= ENSP00000489431.2:p.Asn1268=
ENST00000644379.2:c.3926A= ENSP00000496570.2:p.Asn1309=
ENST00000644555.2:c.647-573A= ENSP00000494614.2:n.647-573A=
ENST00000652672.2:c.3785A= ENSP00000498906.2:p.Asn1262=
ENST00000484087.6:c.665-573A= ENSP00000419481.2:n.665-573A=
ENST00000700182.1:c.707-573A= ENSP00000514849.1:n.707-573A=
ENST00000357654.9:c.3926A= MANE Select ENSP00000350283.3:p.Asn1309=
ENST00000471181.7:c.3926A= ENSP00000418960.2:p.Asn1309=
ENST00000644379.1:c.247A=
ENST00000352993.7:c.671-573A= ENSP00000312236.5:n.671-573A=
ENST00000354071.7:c.3926A= ENSP00000326002.7:p.Asn1309=
ENST00000357654.7:c.3926A= ENSP00000350283.3:p.Asn1309=
ENST00000461221.5:c.*3709A= ENSP00000418548.1:n.*3709A=
ENST00000461574.1:c.220A=
ENST00000468300.5:c.788-573A= ENSP00000417148.1:n.788-573A=
ENST00000471181.6:c.3926A= ENSP00000418960.2:p.Asn1309=
ENST00000478531.5:c.785-573A= ENSP00000420412.1:n.785-573A=
ENST00000484087.5:c.410-573A= ENSP00000419481.1:n.410-573A=
ENST00000487825.5:c.413-573A= ENSP00000418212.1:n.413-573A=
ENST00000491747.6:c.788-573A= ENSP00000420705.2:n.788-573A=
ENST00000493795.5:c.3785A= ENSP00000418775.1:p.Asn1262=
ENST00000493919.5:c.647-573A= ENSP00000418819.1:n.647-573A=
ENST00000586385.5:c.5-27654A= ENSP00000465818.1:n.5-27654A=
ENST00000591534.5:c.-43-17084A= ENSP00000467329.1:n.-43-17084A=
ENST00000591849.5:c.-99+33666A= ENSP00000465347.1:n.-99+33666A=
NM_007294.3:c.3926A= , LRG_292t1:c.3926A= NP_009225.1:p.Asn1309=
NM_007297.3:c.3785A= NP_009228.2:p.Asn1262=
NM_007298.3:c.788-573A= NP_009229.2:n.788-573A=
NM_007299.3:c.788-573A= NP_009230.2:n.788-573A=
NM_007300.3:c.3926A= NP_009231.2:p.Asn1309=
NR_027676.1:n.4062A=
NM_007294.4:c.3926A= MANE Select NP_009225.1:p.Asn1309=
NM_007297.4:c.3785A= NP_009228.2:p.Asn1262=
NM_007299.4:c.788-573A= NP_009230.2:n.788-573A=
NM_007300.4:c.3926A= NP_009231.2:p.Asn1309=
NR_027676.2:n.4103A=