Canonical Allele Identifier: CA2260771315
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43067614T= , CM000679.2:g.43067614T= GRCh38
NC_000017.10:g.41219631T= , CM000679.1:g.41219631T= GRCh37
NC_000017.9:g.38473157T= NCBI36
NG_005905.2:g.150370A= , LRG_292:g.150370A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5065A= ENSP00000417241.2:p.Lys1689=
ENST00000470026.6:c.5068A= ENSP00000419274.2:p.Lys1690=
ENST00000473961.6:c.4942A= ENSP00000420201.2:p.Lys1648=
ENST00000476777.6:c.5062A= ENSP00000417554.2:p.Lys1688=
ENST00000477152.6:c.4990A= ENSP00000419988.2:p.Lys1664=
ENST00000478531.6:c.1756A= ENSP00000420412.2:p.Lys586=
ENST00000489037.2:c.4990A= ENSP00000420781.2:p.Lys1664=
ENST00000493919.6:c.1618A= ENSP00000418819.2:p.Lys540=
ENST00000494123.6:c.5068A= ENSP00000419103.2:p.Lys1690=
ENST00000497488.2:c.4180A= ENSP00000418986.2:p.Lys1394=
ENST00000618469.2:c.5068A= ENSP00000478114.2:p.Lys1690=
ENST00000634433.2:c.4945A= ENSP00000489431.2:p.Lys1649=
ENST00000644379.2:c.5134A= ENSP00000496570.2:p.Lys1712=
ENST00000644555.2:c.1618A= ENSP00000494614.2:p.Lys540=
ENST00000652672.2:c.4927A= ENSP00000498906.2:p.Lys1643=
ENST00000484087.6:c.1630A= ENSP00000419481.2:p.Lys544=
ENST00000357654.9:c.5068A= MANE Select ENSP00000350283.3:p.Lys1690=
ENST00000471181.7:c.5131A= ENSP00000418960.2:p.Lys1711=
ENST00000644379.1:c.1455A=
ENST00000352993.7:c.1642A= ENSP00000312236.5:p.Lys548=
ENST00000357654.7:c.5068A= ENSP00000350283.3:p.Lys1690=
ENST00000461221.5:c.*4851A= ENSP00000418548.1:n.*4851A=
ENST00000468300.5:c.1756A= ENSP00000417148.1:p.Lys586=
ENST00000471181.6:c.5131A= ENSP00000418960.2:p.Lys1711=
ENST00000472490.1:n.221A=
ENST00000478531.5:c.1756A= ENSP00000420412.1:p.Lys586=
ENST00000484087.5:c.1381A= ENSP00000419481.1:p.Lys461=
ENST00000491747.6:c.1756A= ENSP00000420705.2:p.Lys586=
ENST00000493795.5:c.4927A= ENSP00000418775.1:p.Lys1643=
ENST00000493919.5:c.1618A= ENSP00000418819.1:p.Lys540=
ENST00000586385.5:c.5-3663A= ENSP00000465818.1:n.5-3663A=
ENST00000591534.5:c.541A= ENSP00000467329.1:p.Lys181=
ENST00000591849.5:c.-98-17424A= ENSP00000465347.1:n.-98-17424A=
NM_007294.3:c.5068A= , LRG_292t1:c.5068A= NP_009225.1:p.Lys1690=
NM_007297.3:c.4927A= NP_009228.2:p.Lys1643=
NM_007298.3:c.1756A= NP_009229.2:p.Lys586=
NM_007299.3:c.1756A= NP_009230.2:p.Lys586=
NM_007300.3:c.5131A= NP_009231.2:p.Lys1711=
NR_027676.1:n.5204A=
NM_007294.4:c.5068A= MANE Select NP_009225.1:p.Lys1690=
NM_007297.4:c.4927A= NP_009228.2:p.Lys1643=
NM_007299.4:c.1756A= NP_009230.2:p.Lys586=
NM_007300.4:c.5131A= NP_009231.2:p.Lys1711=
NR_027676.2:n.5245A=