Canonical Allele Identifier: CA2260761160
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43045800T= , CM000679.2:g.43045800T= GRCh38
NC_000017.10:g.41197817T= , CM000679.1:g.41197817T= GRCh37
NC_000017.9:g.38451343T= NCBI36
NG_005905.2:g.172184A= , LRG_292:g.172184A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5467A= ENSP00000417241.2:p.Ile1823=
ENST00000470026.6:c.5470A= ENSP00000419274.2:p.Ile1824=
ENST00000473961.6:c.5344A= ENSP00000420201.2:p.Ile1782=
ENST00000476777.6:c.5464A= ENSP00000417554.2:p.Ile1822=
ENST00000477152.6:c.5392A= ENSP00000419988.2:p.Ile1798=
ENST00000478531.6:c.2158A= ENSP00000420412.2:p.Ile720=
ENST00000489037.2:c.5392A= ENSP00000420781.2:p.Ile1798=
ENST00000493919.6:c.2020A= ENSP00000418819.2:p.Ile674=
ENST00000494123.6:c.5470A= ENSP00000419103.2:p.Ile1824=
ENST00000497488.2:c.4582A= ENSP00000418986.2:p.Ile1528=
ENST00000618469.2:c.5470A= ENSP00000478114.2:p.Ile1824=
ENST00000634433.2:c.5347A= ENSP00000489431.2:p.Ile1783=
ENST00000644379.2:c.5536A= ENSP00000496570.2:p.Ile1846=
ENST00000644555.2:c.2020A= ENSP00000494614.2:p.Ile674=
ENST00000652672.2:c.5329A= ENSP00000498906.2:p.Ile1777=
ENST00000484087.6:c.2032A= ENSP00000419481.2:p.Ile678=
ENST00000700081.1:n.1353A=
ENST00000700082.1:n.834A=
ENST00000357654.9:c.5470A= MANE Select ENSP00000350283.3:p.Ile1824=
ENST00000471181.7:c.5533A= ENSP00000418960.2:p.Ile1845=
ENST00000644379.1:c.1857A=
ENST00000352993.7:c.2044A= ENSP00000312236.5:p.Ile682=
ENST00000357654.7:c.5470A= ENSP00000350283.3:p.Ile1824=
ENST00000461221.5:c.*5253A= ENSP00000418548.1:n.*5253A=
ENST00000468300.5:c.2084A= ENSP00000417148.1:p.Asn695=
ENST00000471181.6:c.5533A= ENSP00000418960.2:p.Ile1845=
ENST00000491747.6:c.2158A= ENSP00000420705.2:p.Ile720=
ENST00000493795.5:c.5329A= ENSP00000418775.1:p.Ile1777=
ENST00000586385.5:c.400A= ENSP00000465818.1:p.Ile134=
ENST00000591534.5:c.943A= ENSP00000467329.1:p.Ile315=
ENST00000591849.5:c.169A= ENSP00000465347.1:p.Ile57=
NM_007294.3:c.5470A= , LRG_292t1:c.5470A= NP_009225.1:p.Ile1824=
NM_007297.3:c.5329A= NP_009228.2:p.Ile1777=
NM_007298.3:c.2158A= NP_009229.2:p.Ile720=
NM_007299.3:c.2084A= NP_009230.2:p.Asn695=
NM_007300.3:c.5533A= NP_009231.2:p.Ile1845=
NR_027676.1:n.5606A=
NM_007294.4:c.5470A= MANE Select NP_009225.1:p.Ile1824=
NM_007297.4:c.5329A= NP_009228.2:p.Ile1777=
NM_007299.4:c.2084A= NP_009230.2:p.Asn695=
NM_007300.4:c.5533A= NP_009231.2:p.Ile1845=
NR_027676.2:n.5647A=