Canonical Allele Identifier: CA2260775420
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43076447G= , CM000679.2:g.43076447G= GRCh38
NC_000017.10:g.41228464G= , CM000679.1:g.41228464G= GRCh37
NC_000017.9:g.38481990G= NCBI36
NG_005905.2:g.141537C= , LRG_292:g.141537C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.4481+41C= ENSP00000417241.2:n.4481+41C=
ENST00000470026.6:c.4484+41C= ENSP00000419274.2:n.4484+41C=
ENST00000473961.6:c.4358+41C= ENSP00000420201.2:n.4358+41C=
ENST00000476777.6:c.4478+41C= ENSP00000417554.2:n.4478+41C=
ENST00000477152.6:c.4406+41C= ENSP00000419988.2:n.4406+41C=
ENST00000478531.6:c.1172+41C= ENSP00000420412.2:n.1172+41C=
ENST00000489037.2:c.4406+41C= ENSP00000420781.2:n.4406+41C=
ENST00000493919.6:c.1034+41C= ENSP00000418819.2:n.1034+41C=
ENST00000494123.6:c.4484+41C= ENSP00000419103.2:n.4484+41C=
ENST00000497488.2:c.3596+41C= ENSP00000418986.2:n.3596+41C=
ENST00000618469.2:c.4484+41C= ENSP00000478114.2:n.4484+41C=
ENST00000634433.2:c.4361+41C= ENSP00000489431.2:n.4361+41C=
ENST00000644379.2:c.4550+41C= ENSP00000496570.2:n.4550+41C=
ENST00000644555.2:c.1034+41C= ENSP00000494614.2:n.1034+41C=
ENST00000652672.2:c.4343+41C= ENSP00000498906.2:n.4343+41C=
ENST00000484087.6:c.1046+41C= ENSP00000419481.2:n.1046+41C=
ENST00000700182.1:c.1091+41C= ENSP00000514849.1:n.1091+41C=
ENST00000357654.9:c.4484+41C= MANE Select ENSP00000350283.3:n.4484+41C=
ENST00000471181.7:c.4547+41C= ENSP00000418960.2:n.4547+41C=
ENST00000644379.1:c.871+41C=
ENST00000352993.7:c.1058+41C= ENSP00000312236.5:n.1058+41C=
ENST00000357654.7:c.4484+41C= ENSP00000350283.3:n.4484+41C=
ENST00000461221.5:c.*4267+41C= ENSP00000418548.1:n.*4267+41C=
ENST00000468300.5:c.1172+41C= ENSP00000417148.1:n.1172+41C=
ENST00000471181.6:c.4547+41C= ENSP00000418960.2:n.4547+41C=
ENST00000478531.5:c.1172+41C= ENSP00000420412.1:n.1172+41C=
ENST00000484087.5:c.797+41C= ENSP00000419481.1:n.797+41C=
ENST00000491747.6:c.1172+41C= ENSP00000420705.2:n.1172+41C=
ENST00000493795.5:c.4343+41C= ENSP00000418775.1:n.4343+41C=
ENST00000493919.5:c.1034+41C= ENSP00000418819.1:n.1034+41C=
ENST00000586385.5:c.5-12496C= ENSP00000465818.1:n.5-12496C=
ENST00000591534.5:c.-43-1926C= ENSP00000467329.1:n.-43-1926C=
ENST00000591849.5:c.-98-26257C= ENSP00000465347.1:n.-98-26257C=
NM_007294.3:c.4484+41C= , LRG_292t1:c.4484+41C= NP_009225.1:n.4484+41C=
NM_007297.3:c.4343+41C= NP_009228.2:n.4343+41C=
NM_007298.3:c.1172+41C= NP_009229.2:n.1172+41C=
NM_007299.3:c.1172+41C= NP_009230.2:n.1172+41C=
NM_007300.3:c.4547+41C= NP_009231.2:n.4547+41C=
NR_027676.1:n.4620+41C=
NM_007294.4:c.4484+41C= MANE Select NP_009225.1:n.4484+41C=
NM_007297.4:c.4343+41C= NP_009228.2:n.4343+41C=
NM_007299.4:c.1172+41C= NP_009230.2:n.1172+41C=
NM_007300.4:c.4547+41C= NP_009231.2:n.4547+41C=
NR_027676.2:n.4661+41C=