Canonical Allele Identifier: CA2260761006
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43045686G= , CM000679.2:g.43045686G= GRCh38
NC_000017.10:g.41197703G= , CM000679.1:g.41197703G= GRCh37
NC_000017.9:g.38451229G= NCBI36
NG_005905.2:g.172298C= , LRG_292:g.172298C=

Transcript Alleles

HGVS Amino-acid change
ENST00000461574.2:c.5581C= ENSP00000417241.2:p.His1861=
ENST00000470026.6:c.5584C= ENSP00000419274.2:p.His1862=
ENST00000473961.6:c.5458C= ENSP00000420201.2:p.His1820=
ENST00000476777.6:c.5578C= ENSP00000417554.2:p.His1860=
ENST00000477152.6:c.5506C= ENSP00000419988.2:p.His1836=
ENST00000478531.6:c.2272C= ENSP00000420412.2:p.His758=
ENST00000489037.2:c.5506C= ENSP00000420781.2:p.His1836=
ENST00000493919.6:c.2134C= ENSP00000418819.2:p.His712=
ENST00000494123.6:c.5584C= ENSP00000419103.2:p.His1862=
ENST00000497488.2:c.4696C= ENSP00000418986.2:p.His1566=
ENST00000618469.2:c.5584C= ENSP00000478114.2:p.His1862=
ENST00000634433.2:c.5461C= ENSP00000489431.2:p.His1821=
ENST00000644379.2:c.5650C= ENSP00000496570.2:p.His1884=
ENST00000644555.2:c.2134C= ENSP00000494614.2:p.His712=
ENST00000652672.2:c.5443C= ENSP00000498906.2:p.His1815=
ENST00000484087.6:c.2146C= ENSP00000419481.2:p.His716=
ENST00000700081.1:n.1467C=
ENST00000700082.1:n.948C=
ENST00000357654.9:c.5584C= MANE Select ENSP00000350283.3:p.His1862=
ENST00000471181.7:c.5647C= ENSP00000418960.2:p.His1883=
ENST00000644379.1:c.1971C=
ENST00000352993.7:c.2158C= ENSP00000312236.5:p.His720=
ENST00000357654.7:c.5584C= ENSP00000350283.3:p.His1862=
ENST00000461221.5:c.*5367C= ENSP00000418548.1:n.*5367C=
ENST00000468300.5:c.*98C= ENSP00000417148.1:n.*98C=
ENST00000471181.6:c.5647C= ENSP00000418960.2:p.His1883=
ENST00000491747.6:c.2272C= ENSP00000420705.2:p.His758=
ENST00000493795.5:c.5443C= ENSP00000418775.1:p.His1815=
ENST00000586385.5:c.514C= ENSP00000465818.1:p.His172=
ENST00000591534.5:c.1057C= ENSP00000467329.1:p.His353=
ENST00000591849.5:c.283C= ENSP00000465347.1:p.His95=
NM_007294.3:c.5584C= , LRG_292t1:c.5584C= NP_009225.1:p.His1862=
NM_007297.3:c.5443C= NP_009228.2:p.His1815=
NM_007298.3:c.2272C= NP_009229.2:p.His758=
NM_007299.3:c.*98C= NP_009230.2:n.*98C=
NM_007300.3:c.5647C= NP_009231.2:p.His1883=
NR_027676.1:n.5720C=
NM_007294.4:c.5584C= MANE Select NP_009225.1:p.His1862=
NM_007297.4:c.5443C= NP_009228.2:p.His1815=
NM_007299.4:c.*98C= NP_009230.2:n.*98C=
NM_007300.4:c.5647C= NP_009231.2:p.His1883=
NR_027676.2:n.5761C=