Canonical Allele Identifier: CA2260762721
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43049132T= , CM000679.2:g.43049132T= GRCh38
NC_000017.10:g.41201149T= , CM000679.1:g.41201149T= GRCh37
NC_000017.9:g.38454675T= NCBI36
NG_005905.2:g.168852A= , LRG_292:g.168852A=

Transcript Alleles

HGVS Amino-acid change
ENST00000461574.2:c.5392A= ENSP00000417241.2:p.Thr1798=
ENST00000470026.6:c.5395A= ENSP00000419274.2:p.Thr1799=
ENST00000473961.6:c.5269A= ENSP00000420201.2:p.Thr1757=
ENST00000476777.6:c.5389A= ENSP00000417554.2:p.Thr1797=
ENST00000477152.6:c.5317A= ENSP00000419988.2:p.Thr1773=
ENST00000478531.6:c.2083A= ENSP00000420412.2:p.Thr695=
ENST00000489037.2:c.5317A= ENSP00000420781.2:p.Thr1773=
ENST00000493919.6:c.1945A= ENSP00000418819.2:p.Thr649=
ENST00000494123.6:c.5395A= ENSP00000419103.2:p.Thr1799=
ENST00000497488.2:c.4507A= ENSP00000418986.2:p.Thr1503=
ENST00000618469.2:c.5395A= ENSP00000478114.2:p.Thr1799=
ENST00000634433.2:c.5272A= ENSP00000489431.2:p.Thr1758=
ENST00000644379.2:c.5461A= ENSP00000496570.2:p.Thr1821=
ENST00000644555.2:c.1945A= ENSP00000494614.2:p.Thr649=
ENST00000652672.2:c.5254A= ENSP00000498906.2:p.Thr1752=
ENST00000484087.6:c.1957A= ENSP00000419481.2:p.Thr653=
ENST00000700081.1:n.1278A=
ENST00000357654.9:c.5395A= MANE Select ENSP00000350283.3:p.Thr1799=
ENST00000471181.7:c.5458A= ENSP00000418960.2:p.Thr1820=
ENST00000644379.1:c.1782A=
ENST00000352993.7:c.1969A= ENSP00000312236.5:p.Thr657=
ENST00000357654.7:c.5395A= ENSP00000350283.3:p.Thr1799=
ENST00000461221.5:c.*5178A= ENSP00000418548.1:n.*5178A=
ENST00000468300.5:c.2021-1429A= ENSP00000417148.1:n.2021-1429A=
ENST00000471181.6:c.5458A= ENSP00000418960.2:p.Thr1820=
ENST00000491747.6:c.2083A= ENSP00000420705.2:p.Thr695=
ENST00000493795.5:c.5254A= ENSP00000418775.1:p.Thr1752=
ENST00000586385.5:c.325A= ENSP00000465818.1:p.Thr109=
ENST00000591534.5:c.868A= ENSP00000467329.1:p.Thr290=
ENST00000591849.5:c.94A= ENSP00000465347.1:p.Thr32=
NM_007294.3:c.5395A= , LRG_292t1:c.5395A= NP_009225.1:p.Thr1799=
NM_007297.3:c.5254A= NP_009228.2:p.Thr1752=
NM_007298.3:c.2083A= NP_009229.2:p.Thr695=
NM_007299.3:c.2021-1429A= NP_009230.2:n.2021-1429A=
NM_007300.3:c.5458A= NP_009231.2:p.Thr1820=
NR_027676.1:n.5531A=
NM_007294.4:c.5395A= MANE Select NP_009225.1:p.Thr1799=
NM_007297.4:c.5254A= NP_009228.2:p.Thr1752=
NM_007299.4:c.2021-1429A= NP_009230.2:n.2021-1429A=
NM_007300.4:c.5458A= NP_009231.2:p.Thr1820=
NR_027676.2:n.5572A=