Canonical Allele Identifier: CA626078998
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1058977
dbSNP Id: rs1360158770

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43057153_43057154del , CM000679.2:g.43057153_43057154del GRCh38
NC_000017.10:g.41209170_41209171del , CM000679.1:g.41209170_41209171del GRCh37
NC_000017.9:g.38462696_38462697del NCBI36
NG_005905.2:g.160833_160834del , LRG_292:g.160833_160834del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5191-16_5191-15del ENSP00000417241.2:n.5191-16_5191-15del
ENST00000470026.6:c.5194-16_5194-15del ENSP00000419274.2:n.5194-16_5194-15del
ENST00000473961.6:c.5068-16_5068-15del ENSP00000420201.2:n.5068-16_5068-15del
ENST00000476777.6:c.5188-16_5188-15del ENSP00000417554.2:n.5188-16_5188-15del
ENST00000477152.6:c.5116-16_5116-15del ENSP00000419988.2:n.5116-16_5116-15del
ENST00000478531.6:c.1882-16_1882-15del ENSP00000420412.2:n.1882-16_1882-15del
ENST00000489037.2:c.5116-16_5116-15del ENSP00000420781.2:n.5116-16_5116-15del
ENST00000493919.6:c.1744-16_1744-15del ENSP00000418819.2:n.1744-16_1744-15del
ENST00000494123.6:c.5194-16_5194-15del ENSP00000419103.2:n.5194-16_5194-15del
ENST00000497488.2:c.4306-16_4306-15del ENSP00000418986.2:n.4306-16_4306-15del
ENST00000618469.2:c.5194-16_5194-15del ENSP00000478114.2:n.5194-16_5194-15del
ENST00000634433.2:c.5071-16_5071-15del ENSP00000489431.2:n.5071-16_5071-15del
ENST00000644379.2:c.5260-16_5260-15del ENSP00000496570.2:n.5260-16_5260-15del
ENST00000644555.2:c.1744-16_1744-15del ENSP00000494614.2:n.1744-16_1744-15del
ENST00000652672.2:c.5053-16_5053-15del ENSP00000498906.2:n.5053-16_5053-15del
ENST00000484087.6:c.1756-16_1756-15del ENSP00000419481.2:n.1756-16_1756-15del
ENST00000357654.9:c.5194-16_5194-15del MANE Select ENSP00000350283.3:n.5194-16_5194-15del
ENST00000471181.7:c.5257-16_5257-15del ENSP00000418960.2:n.5257-16_5257-15del
ENST00000644379.1:c.1581-16_1581-15del
ENST00000352993.7:c.1768-16_1768-15del ENSP00000312236.5:n.1768-16_1768-15del
ENST00000357654.7:c.5194-16_5194-15del ENSP00000350283.3:n.5194-16_5194-15del
ENST00000461221.5:c.*4977-16_*4977-15del ENSP00000418548.1:n.*4977-16_*4977-15del
ENST00000468300.5:c.1882-16_1882-15del ENSP00000417148.1:n.1882-16_1882-15del
ENST00000471181.6:c.5257-16_5257-15del ENSP00000418960.2:n.5257-16_5257-15del
ENST00000491747.6:c.1882-16_1882-15del ENSP00000420705.2:n.1882-16_1882-15del
ENST00000493795.5:c.5053-16_5053-15del ENSP00000418775.1:n.5053-16_5053-15del
ENST00000586385.5:c.124-16_124-15del ENSP00000465818.1:n.124-16_124-15del
ENST00000591534.5:c.667-16_667-15del ENSP00000467329.1:n.667-16_667-15del
ENST00000591849.5:c.-98-6961_-98-6960del ENSP00000465347.1:n.-98-6961_-98-6960del
NM_007294.3:c.5194-16_5194-15del , LRG_292t1:c.5194-16_5194-15del NP_009225.1:n.5194-16_5194-15del
NM_007297.3:c.5053-16_5053-15del NP_009228.2:n.5053-16_5053-15del
NM_007298.3:c.1882-16_1882-15del NP_009229.2:n.1882-16_1882-15del
NM_007299.3:c.1882-16_1882-15del NP_009230.2:n.1882-16_1882-15del
NM_007300.3:c.5257-16_5257-15del NP_009231.2:n.5257-16_5257-15del
NR_027676.1:n.5330-16_5330-15del
NM_007294.4:c.5194-16_5194-15del MANE Select NP_009225.1:n.5194-16_5194-15del
NM_007297.4:c.5053-16_5053-15del NP_009228.2:n.5053-16_5053-15del
NM_007299.4:c.1882-16_1882-15del NP_009230.2:n.1882-16_1882-15del
NM_007300.4:c.5257-16_5257-15del NP_009231.2:n.5257-16_5257-15del
NR_027676.2:n.5371-16_5371-15del