Canonical Allele Identifier: CA10601203
Gene: BRCA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43099855A>T , CM000679.2:g.43099855A>T GRCh38
NC_000017.10:g.41251872A>T , CM000679.1:g.41251872A>T GRCh37
NC_000017.9:g.38505398A>T NCBI36
NG_005905.2:g.118129T>A , LRG_292:g.118129T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.531T>A
ENST00000461574.2:c.467T>A ENSP00000417241.2:p.Leu156His
ENST00000470026.6:c.467T>A ENSP00000419274.2:p.Leu156His
ENST00000473961.6:c.464T>A ENSP00000420201.2:p.Leu155His
ENST00000476777.6:c.464T>A ENSP00000417554.2:p.Leu155His
ENST00000477152.6:c.389T>A ENSP00000419988.2:p.Leu130His
ENST00000478531.6:c.464T>A ENSP00000420412.2:p.Leu155His
ENST00000489037.2:c.389T>A ENSP00000420781.2:p.Leu130His
ENST00000493919.6:c.326T>A ENSP00000418819.2:p.Leu109His
ENST00000494123.6:c.467T>A ENSP00000419103.2:p.Leu156His
ENST00000497488.2:c.-218-4995T>A ENSP00000418986.2:n.-218-4995T>A
ENST00000618469.2:c.467T>A ENSP00000478114.2:p.Leu156His
ENST00000634433.2:c.467T>A ENSP00000489431.2:p.Leu156His
ENST00000644379.2:c.467T>A ENSP00000496570.2:p.Leu156His
ENST00000644555.2:c.326T>A ENSP00000494614.2:p.Leu109His
ENST00000652672.2:c.326T>A ENSP00000498906.2:p.Leu109His
ENST00000484087.6:c.467T>A ENSP00000419481.2:p.Leu156His
ENST00000700182.1:c.386T>A ENSP00000514849.1:p.Leu129His
ENST00000700183.1:c.*381T>A ENSP00000514850.1:n.*381T>A
ENST00000700184.1:n.707T>A
ENST00000357654.9:c.467T>A MANE Select ENSP00000350283.3:p.Leu156His
ENST00000471181.7:c.467T>A ENSP00000418960.2:p.Leu156His
ENST00000642945.1:c.*341T>A ENSP00000495897.1:n.*341T>A
ENST00000652672.1:c.326T>A ENSP00000498906.1:p.Leu109His
ENST00000352993.7:c.467T>A ENSP00000312236.5:p.Leu156His
ENST00000354071.7:c.467T>A ENSP00000326002.7:p.Leu156His
ENST00000357654.7:c.467T>A ENSP00000350283.3:p.Leu156His
ENST00000461221.5:c.*250T>A ENSP00000418548.1:n.*250T>A
ENST00000461798.5:c.*253T>A ENSP00000417988.1:n.*253T>A
ENST00000468300.5:c.467T>A ENSP00000417148.1:p.Leu156His
ENST00000470026.5:c.467T>A ENSP00000419274.1:p.Leu156His
ENST00000471181.6:c.467T>A ENSP00000418960.2:p.Leu156His
ENST00000473961.5:c.187T>A
ENST00000476777.5:c.464T>A ENSP00000417554.1:p.Leu155His
ENST00000477152.5:c.389T>A ENSP00000419988.1:p.Leu130His
ENST00000478531.5:c.464T>A ENSP00000420412.1:p.Leu155His
ENST00000484087.5:c.212T>A ENSP00000419481.1:p.Leu71His
ENST00000487825.5:c.215T>A ENSP00000418212.1:p.Leu72His
ENST00000491747.6:c.467T>A ENSP00000420705.2:p.Leu156His
ENST00000492859.5:c.*403T>A ENSP00000420253.1:n.*403T>A
ENST00000493795.5:c.326T>A ENSP00000418775.1:p.Leu109His
ENST00000493919.5:c.326T>A ENSP00000418819.1:p.Leu109His
ENST00000494123.5:c.467T>A ENSP00000419103.1:p.Leu156His
ENST00000497488.1:c.-218-4995T>A ENSP00000418986.1:n.-218-4995T>A
ENST00000586385.5:c.4+25327T>A ENSP00000465818.1:n.4+25327T>A
ENST00000591534.5:c.-43-25334T>A ENSP00000467329.1:n.-43-25334T>A
ENST00000591849.5:c.-99+25416T>A ENSP00000465347.1:n.-99+25416T>A
ENST00000634433.1:c.467T>A ENSP00000489431.1:p.Leu156His
NM_007294.3:c.467T>A , LRG_292t1:c.467T>A NP_009225.1:p.Leu156His
NM_007297.3:c.326T>A NP_009228.2:p.Leu109His
NM_007298.3:c.467T>A NP_009229.2:p.Leu156His
NM_007299.3:c.467T>A NP_009230.2:p.Leu156His
NM_007300.3:c.467T>A NP_009231.2:p.Leu156His
NR_027676.1:n.603T>A
NM_007294.4:c.467T>A MANE Select NP_009225.1:p.Leu156His
NM_007297.4:c.326T>A NP_009228.2:p.Leu109His
NM_007299.4:c.467T>A NP_009230.2:p.Leu156His
NM_007300.4:c.467T>A NP_009231.2:p.Leu156His
NR_027676.2:n.644T>A