Canonical Allele Identifier: CA2260783445
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43092787G= , CM000679.2:g.43092787G= GRCh38
NC_000017.10:g.41244804G= , CM000679.1:g.41244804G= GRCh37
NC_000017.9:g.38498330G= NCBI36
NG_005905.2:g.125197C= , LRG_292:g.125197C=

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.2808C=
ENST00000461574.2:c.2744C= ENSP00000417241.2:p.Ser915=
ENST00000470026.6:c.2744C= ENSP00000419274.2:p.Ser915=
ENST00000473961.6:c.2618C= ENSP00000420201.2:p.Ser873=
ENST00000476777.6:c.2741C= ENSP00000417554.2:p.Ser914=
ENST00000477152.6:c.2666C= ENSP00000419988.2:p.Ser889=
ENST00000478531.6:c.785-1755C= ENSP00000420412.2:n.785-1755C=
ENST00000489037.2:c.2666C= ENSP00000420781.2:p.Ser889=
ENST00000493919.6:c.647-1755C= ENSP00000418819.2:n.647-1755C=
ENST00000494123.6:c.2744C= ENSP00000419103.2:p.Ser915=
ENST00000497488.2:c.1856C= ENSP00000418986.2:p.Ser619=
ENST00000618469.2:c.2744C= ENSP00000478114.2:p.Ser915=
ENST00000634433.2:c.2621C= ENSP00000489431.2:p.Ser874=
ENST00000644379.2:c.2744C= ENSP00000496570.2:p.Ser915=
ENST00000644555.2:c.647-1755C= ENSP00000494614.2:n.647-1755C=
ENST00000652672.2:c.2603C= ENSP00000498906.2:p.Ser868=
ENST00000484087.6:c.665-1755C= ENSP00000419481.2:n.665-1755C=
ENST00000700182.1:c.707-1755C= ENSP00000514849.1:n.707-1755C=
ENST00000357654.9:c.2744C= MANE Select ENSP00000350283.3:p.Ser915=
ENST00000471181.7:c.2744C= ENSP00000418960.2:p.Ser915=
ENST00000352993.7:c.671-1755C= ENSP00000312236.5:n.671-1755C=
ENST00000354071.7:c.2744C= ENSP00000326002.7:p.Ser915=
ENST00000357654.7:c.2744C= ENSP00000350283.3:p.Ser915=
ENST00000461221.5:c.*2527C= ENSP00000418548.1:n.*2527C=
ENST00000468300.5:c.788-1755C= ENSP00000417148.1:n.788-1755C=
ENST00000471181.6:c.2744C= ENSP00000418960.2:p.Ser915=
ENST00000478531.5:c.785-1755C= ENSP00000420412.1:n.785-1755C=
ENST00000484087.5:c.410-1755C= ENSP00000419481.1:n.410-1755C=
ENST00000487825.5:c.413-1755C= ENSP00000418212.1:n.413-1755C=
ENST00000491747.6:c.788-1755C= ENSP00000420705.2:n.788-1755C=
ENST00000493795.5:c.2603C= ENSP00000418775.1:p.Ser868=
ENST00000493919.5:c.647-1755C= ENSP00000418819.1:n.647-1755C=
ENST00000586385.5:c.5-28836C= ENSP00000465818.1:n.5-28836C=
ENST00000591534.5:c.-43-18266C= ENSP00000467329.1:n.-43-18266C=
ENST00000591849.5:c.-99+32484C= ENSP00000465347.1:n.-99+32484C=
NM_007294.3:c.2744C= , LRG_292t1:c.2744C= NP_009225.1:p.Ser915=
NM_007297.3:c.2603C= NP_009228.2:p.Ser868=
NM_007298.3:c.788-1755C= NP_009229.2:n.788-1755C=
NM_007299.3:c.788-1755C= NP_009230.2:n.788-1755C=
NM_007300.3:c.2744C= NP_009231.2:p.Ser915=
NR_027676.1:n.2880C=
NM_007294.4:c.2744C= MANE Select NP_009225.1:p.Ser915=
NM_007297.4:c.2603C= NP_009228.2:p.Ser868=
NM_007299.4:c.788-1755C= NP_009230.2:n.788-1755C=
NM_007300.4:c.2744C= NP_009231.2:p.Ser915=
NR_027676.2:n.2921C=