Canonical Allele Identifier: CA2260777992
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43082457T= , CM000679.2:g.43082457T= GRCh38
NC_000017.10:g.41234474T= , CM000679.1:g.41234474T= GRCh37
NC_000017.9:g.38488000T= NCBI36
NG_005905.2:g.135527A= , LRG_292:g.135527A=

Transcript Alleles

HGVS Amino-acid change
ENST00000461574.2:c.4304A= ENSP00000417241.2:p.Asp1435=
ENST00000470026.6:c.4304A= ENSP00000419274.2:p.Asp1435=
ENST00000473961.6:c.4178A= ENSP00000420201.2:p.Asp1393=
ENST00000476777.6:c.4298A= ENSP00000417554.2:p.Asp1433=
ENST00000477152.6:c.4226A= ENSP00000419988.2:p.Asp1409=
ENST00000478531.6:c.992A= ENSP00000420412.2:p.Asp331=
ENST00000489037.2:c.4226A= ENSP00000420781.2:p.Asp1409=
ENST00000493919.6:c.854A= ENSP00000418819.2:p.Asp285=
ENST00000494123.6:c.4304A= ENSP00000419103.2:p.Asp1435=
ENST00000497488.2:c.3416A= ENSP00000418986.2:p.Asp1139=
ENST00000618469.2:c.4304A= ENSP00000478114.2:p.Asp1435=
ENST00000634433.2:c.4181A= ENSP00000489431.2:p.Asp1394=
ENST00000644379.2:c.4304A= ENSP00000496570.2:p.Asp1435=
ENST00000644555.2:c.854A= ENSP00000494614.2:p.Asp285=
ENST00000652672.2:c.4163A= ENSP00000498906.2:p.Asp1388=
ENST00000484087.6:c.869A= ENSP00000419481.2:p.Asp290=
ENST00000700182.1:c.914A= ENSP00000514849.1:p.Asp305=
ENST00000357654.9:c.4304A= MANE Select ENSP00000350283.3:p.Asp1435=
ENST00000471181.7:c.4304A= ENSP00000418960.2:p.Asp1435=
ENST00000644379.1:c.625A=
ENST00000352993.7:c.878A= ENSP00000312236.5:p.Asp293=
ENST00000357654.7:c.4304A= ENSP00000350283.3:p.Asp1435=
ENST00000461221.5:c.*4087A= ENSP00000418548.1:n.*4087A=
ENST00000461574.1:c.598A=
ENST00000468300.5:c.995A= ENSP00000417148.1:p.Asp332=
ENST00000471181.6:c.4304A= ENSP00000418960.2:p.Asp1435=
ENST00000478531.5:c.992A= ENSP00000420412.1:p.Asp331=
ENST00000484087.5:c.617A= ENSP00000419481.1:p.Asp206=
ENST00000487825.5:c.620A= ENSP00000418212.1:p.Asp207=
ENST00000491747.6:c.995A= ENSP00000420705.2:p.Asp332=
ENST00000493795.5:c.4163A= ENSP00000418775.1:p.Asp1388=
ENST00000493919.5:c.854A= ENSP00000418819.1:p.Asp285=
ENST00000586385.5:c.5-18506A= ENSP00000465818.1:n.5-18506A=
ENST00000591534.5:c.-43-7936A= ENSP00000467329.1:n.-43-7936A=
ENST00000591849.5:c.-98-32267A= ENSP00000465347.1:n.-98-32267A=
ENST00000621897.1:n.198A=
NM_007294.3:c.4304A= , LRG_292t1:c.4304A= NP_009225.1:p.Asp1435=
NM_007297.3:c.4163A= NP_009228.2:p.Asp1388=
NM_007298.3:c.995A= NP_009229.2:p.Asp332=
NM_007299.3:c.995A= NP_009230.2:p.Asp332=
NM_007300.3:c.4304A= NP_009231.2:p.Asp1435=
NR_027676.1:n.4440A=
NM_007294.4:c.4304A= MANE Select NP_009225.1:p.Asp1435=
NM_007297.4:c.4163A= NP_009228.2:p.Asp1388=
NM_007299.4:c.995A= NP_009230.2:p.Asp332=
NM_007300.4:c.4304A= NP_009231.2:p.Asp1435=
NR_027676.2:n.4481A=