Canonical Allele Identifier: CA2260778012
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43082480G= , CM000679.2:g.43082480G= GRCh38
NC_000017.10:g.41234497G= , CM000679.1:g.41234497G= GRCh37
NC_000017.9:g.38488023G= NCBI36
NG_005905.2:g.135504C= , LRG_292:g.135504C=

Transcript Alleles

HGVS Amino-acid change
ENST00000461574.2:c.4281C= ENSP00000417241.2:p.Asn1427=
ENST00000470026.6:c.4281C= ENSP00000419274.2:p.Asn1427=
ENST00000473961.6:c.4155C= ENSP00000420201.2:p.Asn1385=
ENST00000476777.6:c.4275C= ENSP00000417554.2:p.Asn1425=
ENST00000477152.6:c.4203C= ENSP00000419988.2:p.Asn1401=
ENST00000478531.6:c.969C= ENSP00000420412.2:p.Asn323=
ENST00000489037.2:c.4203C= ENSP00000420781.2:p.Asn1401=
ENST00000493919.6:c.831C= ENSP00000418819.2:p.Asn277=
ENST00000494123.6:c.4281C= ENSP00000419103.2:p.Asn1427=
ENST00000497488.2:c.3393C= ENSP00000418986.2:p.Asn1131=
ENST00000618469.2:c.4281C= ENSP00000478114.2:p.Asn1427=
ENST00000634433.2:c.4158C= ENSP00000489431.2:p.Asn1386=
ENST00000644379.2:c.4281C= ENSP00000496570.2:p.Asn1427=
ENST00000644555.2:c.831C= ENSP00000494614.2:p.Asn277=
ENST00000652672.2:c.4140C= ENSP00000498906.2:p.Asn1380=
ENST00000484087.6:c.846C= ENSP00000419481.2:p.Asn282=
ENST00000700182.1:c.891C= ENSP00000514849.1:p.Asn297=
ENST00000357654.9:c.4281C= MANE Select ENSP00000350283.3:p.Asn1427=
ENST00000471181.7:c.4281C= ENSP00000418960.2:p.Asn1427=
ENST00000644379.1:c.602C=
ENST00000352993.7:c.855C= ENSP00000312236.5:p.Asn285=
ENST00000357654.7:c.4281C= ENSP00000350283.3:p.Asn1427=
ENST00000461221.5:c.*4064C= ENSP00000418548.1:n.*4064C=
ENST00000461574.1:c.575C=
ENST00000468300.5:c.972C= ENSP00000417148.1:p.Asn324=
ENST00000471181.6:c.4281C= ENSP00000418960.2:p.Asn1427=
ENST00000478531.5:c.969C= ENSP00000420412.1:p.Asn323=
ENST00000484087.5:c.594C= ENSP00000419481.1:p.Asn198=
ENST00000487825.5:c.597C= ENSP00000418212.1:p.Asn199=
ENST00000491747.6:c.972C= ENSP00000420705.2:p.Asn324=
ENST00000493795.5:c.4140C= ENSP00000418775.1:p.Asn1380=
ENST00000493919.5:c.831C= ENSP00000418819.1:p.Asn277=
ENST00000586385.5:c.5-18529C= ENSP00000465818.1:n.5-18529C=
ENST00000591534.5:c.-43-7959C= ENSP00000467329.1:n.-43-7959C=
ENST00000591849.5:c.-98-32290C= ENSP00000465347.1:n.-98-32290C=
ENST00000621897.1:n.175C=
NM_007294.3:c.4281C= , LRG_292t1:c.4281C= NP_009225.1:p.Asn1427=
NM_007297.3:c.4140C= NP_009228.2:p.Asn1380=
NM_007298.3:c.972C= NP_009229.2:p.Asn324=
NM_007299.3:c.972C= NP_009230.2:p.Asn324=
NM_007300.3:c.4281C= NP_009231.2:p.Asn1427=
NR_027676.1:n.4417C=
NM_007294.4:c.4281C= MANE Select NP_009225.1:p.Asn1427=
NM_007297.4:c.4140C= NP_009228.2:p.Asn1380=
NM_007299.4:c.972C= NP_009230.2:p.Asn324=
NM_007300.4:c.4281C= NP_009231.2:p.Asn1427=
NR_027676.2:n.4458C=