Canonical Allele Identifier: CA2260771319
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43067617T= , CM000679.2:g.43067617T= GRCh38
NC_000017.10:g.41219634T= , CM000679.1:g.41219634T= GRCh37
NC_000017.9:g.38473160T= NCBI36
NG_005905.2:g.150367A= , LRG_292:g.150367A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5062A= ENSP00000417241.2:p.Met1688=
ENST00000470026.6:c.5065A= ENSP00000419274.2:p.Met1689=
ENST00000473961.6:c.4939A= ENSP00000420201.2:p.Met1647=
ENST00000476777.6:c.5059A= ENSP00000417554.2:p.Met1687=
ENST00000477152.6:c.4987A= ENSP00000419988.2:p.Met1663=
ENST00000478531.6:c.1753A= ENSP00000420412.2:p.Met585=
ENST00000489037.2:c.4987A= ENSP00000420781.2:p.Met1663=
ENST00000493919.6:c.1615A= ENSP00000418819.2:p.Met539=
ENST00000494123.6:c.5065A= ENSP00000419103.2:p.Met1689=
ENST00000497488.2:c.4177A= ENSP00000418986.2:p.Met1393=
ENST00000618469.2:c.5065A= ENSP00000478114.2:p.Met1689=
ENST00000634433.2:c.4942A= ENSP00000489431.2:p.Met1648=
ENST00000644379.2:c.5131A= ENSP00000496570.2:p.Met1711=
ENST00000644555.2:c.1615A= ENSP00000494614.2:p.Met539=
ENST00000652672.2:c.4924A= ENSP00000498906.2:p.Met1642=
ENST00000484087.6:c.1627A= ENSP00000419481.2:p.Met543=
ENST00000357654.9:c.5065A= MANE Select ENSP00000350283.3:p.Met1689=
ENST00000471181.7:c.5128A= ENSP00000418960.2:p.Met1710=
ENST00000644379.1:c.1452A=
ENST00000352993.7:c.1639A= ENSP00000312236.5:p.Met547=
ENST00000357654.7:c.5065A= ENSP00000350283.3:p.Met1689=
ENST00000461221.5:c.*4848A= ENSP00000418548.1:n.*4848A=
ENST00000468300.5:c.1753A= ENSP00000417148.1:p.Met585=
ENST00000471181.6:c.5128A= ENSP00000418960.2:p.Met1710=
ENST00000472490.1:n.218A=
ENST00000478531.5:c.1753A= ENSP00000420412.1:p.Met585=
ENST00000484087.5:c.1378A= ENSP00000419481.1:p.Met460=
ENST00000491747.6:c.1753A= ENSP00000420705.2:p.Met585=
ENST00000493795.5:c.4924A= ENSP00000418775.1:p.Met1642=
ENST00000493919.5:c.1615A= ENSP00000418819.1:p.Met539=
ENST00000586385.5:c.5-3666A= ENSP00000465818.1:n.5-3666A=
ENST00000591534.5:c.538A= ENSP00000467329.1:p.Met180=
ENST00000591849.5:c.-98-17427A= ENSP00000465347.1:n.-98-17427A=
NM_007294.3:c.5065A= , LRG_292t1:c.5065A= NP_009225.1:p.Met1689=
NM_007297.3:c.4924A= NP_009228.2:p.Met1642=
NM_007298.3:c.1753A= NP_009229.2:p.Met585=
NM_007299.3:c.1753A= NP_009230.2:p.Met585=
NM_007300.3:c.5128A= NP_009231.2:p.Met1710=
NR_027676.1:n.5201A=
NM_007294.4:c.5065A= MANE Select NP_009225.1:p.Met1689=
NM_007297.4:c.4924A= NP_009228.2:p.Met1642=
NM_007299.4:c.1753A= NP_009230.2:p.Met585=
NM_007300.4:c.5128A= NP_009231.2:p.Met1710=
NR_027676.2:n.5242A=