Canonical Allele Identifier: CA2733673775
Gene: BRCA1 HGNC NCBI

Linked Data

dbSNP Id: rs1443698959

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43045582G>C , CM000679.2:g.43045582G>C GRCh38
NC_000017.10:g.41197599G>C , CM000679.1:g.41197599G>C GRCh37
NC_000017.9:g.38451125G>C NCBI36
NG_005905.2:g.172402C>G , LRG_292:g.172402C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000461574.2:c.*96C>G ENSP00000417241.2:n.*96C>G
ENST00000470026.6:c.*96C>G ENSP00000419274.2:n.*96C>G
ENST00000473961.6:c.*96C>G ENSP00000420201.2:n.*96C>G
ENST00000476777.6:c.*96C>G ENSP00000417554.2:n.*96C>G
ENST00000477152.6:c.*96C>G ENSP00000419988.2:n.*96C>G
ENST00000478531.6:c.*96C>G ENSP00000420412.2:n.*96C>G
ENST00000489037.2:c.*96C>G ENSP00000420781.2:n.*96C>G
ENST00000493919.6:c.*96C>G ENSP00000418819.2:n.*96C>G
ENST00000494123.6:c.*96C>G ENSP00000419103.2:n.*96C>G
ENST00000497488.2:c.*96C>G ENSP00000418986.2:n.*96C>G
ENST00000618469.2:c.*96C>G ENSP00000478114.2:n.*96C>G
ENST00000634433.2:c.*96C>G ENSP00000489431.2:n.*96C>G
ENST00000644379.2:c.*96C>G ENSP00000496570.2:n.*96C>G
ENST00000644555.2:c.*96C>G ENSP00000494614.2:n.*96C>G
ENST00000652672.2:c.*96C>G ENSP00000498906.2:n.*96C>G
ENST00000484087.6:c.*96C>G ENSP00000419481.2:n.*96C>G
ENST00000700081.1:n.1571C>G
ENST00000700082.1:n.1052C>G
ENST00000357654.9:c.*96C>G MANE Select ENSP00000350283.3:n.*96C>G
ENST00000471181.7:c.*96C>G ENSP00000418960.2:n.*96C>G
ENST00000644379.1:c.2075C>G
ENST00000352993.7:c.*96C>G ENSP00000312236.5:n.*96C>G
ENST00000357654.7:c.*96C>G ENSP00000350283.3:n.*96C>G
ENST00000468300.5:c.*202C>G ENSP00000417148.1:n.*202C>G
ENST00000586385.5:c.*96C>G ENSP00000465818.1:n.*96C>G
ENST00000591534.5:c.*96C>G ENSP00000467329.1:n.*96C>G
ENST00000591849.5:c.*96C>G ENSP00000465347.1:n.*96C>G
NM_007294.3:c.*96C>G , LRG_292t1:c.*96C>G NP_009225.1:n.*96C>G
NM_007297.3:c.*96C>G NP_009228.2:n.*96C>G
NM_007298.3:c.*96C>G NP_009229.2:n.*96C>G
NM_007299.3:c.*202C>G NP_009230.2:n.*202C>G
NM_007300.3:c.*96C>G NP_009231.2:n.*96C>G
NR_027676.1:n.5824C>G
NM_007294.4:c.*96C>G MANE Select NP_009225.1:n.*96C>G
NM_007297.4:c.*96C>G NP_009228.2:n.*96C>G
NM_007299.4:c.*202C>G NP_009230.2:n.*202C>G
NM_007300.4:c.*96C>G NP_009231.2:n.*96C>G
NR_027676.2:n.5865C>G