Canonical Allele Identifier: CA2260762840
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43049252C= , CM000679.2:g.43049252C= GRCh38
NC_000017.10:g.41201269C= , CM000679.1:g.41201269C= GRCh37
NC_000017.9:g.38454795C= NCBI36
NG_005905.2:g.168732G= , LRG_292:g.168732G=

Transcript Alleles

HGVS Amino-acid change
ENST00000461574.2:c.5330-58G= ENSP00000417241.2:n.5330-58G=
ENST00000470026.6:c.5333-58G= ENSP00000419274.2:n.5333-58G=
ENST00000473961.6:c.5207-58G= ENSP00000420201.2:n.5207-58G=
ENST00000476777.6:c.5327-58G= ENSP00000417554.2:n.5327-58G=
ENST00000477152.6:c.5255-58G= ENSP00000419988.2:n.5255-58G=
ENST00000478531.6:c.2021-58G= ENSP00000420412.2:n.2021-58G=
ENST00000489037.2:c.5255-58G= ENSP00000420781.2:n.5255-58G=
ENST00000493919.6:c.1883-58G= ENSP00000418819.2:n.1883-58G=
ENST00000494123.6:c.5333-58G= ENSP00000419103.2:n.5333-58G=
ENST00000497488.2:c.4445-58G= ENSP00000418986.2:n.4445-58G=
ENST00000618469.2:c.5333-58G= ENSP00000478114.2:n.5333-58G=
ENST00000634433.2:c.5210-58G= ENSP00000489431.2:n.5210-58G=
ENST00000644379.2:c.5399-58G= ENSP00000496570.2:n.5399-58G=
ENST00000644555.2:c.1883-58G= ENSP00000494614.2:n.1883-58G=
ENST00000652672.2:c.5192-58G= ENSP00000498906.2:n.5192-58G=
ENST00000484087.6:c.1895-58G= ENSP00000419481.2:n.1895-58G=
ENST00000700081.1:n.1158G=
ENST00000357654.9:c.5333-58G= MANE Select ENSP00000350283.3:n.5333-58G=
ENST00000471181.7:c.5396-58G= ENSP00000418960.2:n.5396-58G=
ENST00000644379.1:c.1720-58G=
ENST00000352993.7:c.1907-58G= ENSP00000312236.5:n.1907-58G=
ENST00000357654.7:c.5333-58G= ENSP00000350283.3:n.5333-58G=
ENST00000461221.5:c.*5116-58G= ENSP00000418548.1:n.*5116-58G=
ENST00000468300.5:c.2021-1549G= ENSP00000417148.1:n.2021-1549G=
ENST00000471181.6:c.5396-58G= ENSP00000418960.2:n.5396-58G=
ENST00000491747.6:c.2021-58G= ENSP00000420705.2:n.2021-58G=
ENST00000493795.5:c.5192-58G= ENSP00000418775.1:n.5192-58G=
ENST00000586385.5:c.263-58G= ENSP00000465818.1:n.263-58G=
ENST00000591534.5:c.806-58G= ENSP00000467329.1:n.806-58G=
ENST00000591849.5:c.32-58G= ENSP00000465347.1:n.32-58G=
NM_007294.3:c.5333-58G= , LRG_292t1:c.5333-58G= NP_009225.1:n.5333-58G=
NM_007297.3:c.5192-58G= NP_009228.2:n.5192-58G=
NM_007298.3:c.2021-58G= NP_009229.2:n.2021-58G=
NM_007299.3:c.2021-1549G= NP_009230.2:n.2021-1549G=
NM_007300.3:c.5396-58G= NP_009231.2:n.5396-58G=
NR_027676.1:n.5469-58G=
NM_007294.4:c.5333-58G= MANE Select NP_009225.1:n.5333-58G=
NM_007297.4:c.5192-58G= NP_009228.2:n.5192-58G=
NM_007299.4:c.2021-1549G= NP_009230.2:n.2021-1549G=
NM_007300.4:c.5396-58G= NP_009231.2:n.5396-58G=
NR_027676.2:n.5510-58G=