Canonical Allele Identifier: CA003628
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 55591
dbSNP Id: rs80357973

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43045796_43045803del , CM000679.2:g.43045796_43045803del GRCh38
NC_000017.10:g.41197813_41197820del , CM000679.1:g.41197813_41197820del GRCh37
NC_000017.9:g.38451339_38451346del NCBI36
NG_005905.2:g.172184_172191del , LRG_292:g.172184_172191del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5467_5474del
ENST00000470026.6:c.5470_5477del
ENST00000473961.6:c.5344_5351del
ENST00000476777.6:c.5464_5471del
ENST00000477152.6:c.5392_5399del
ENST00000478531.6:c.2158_2165del
ENST00000489037.2:c.5392_5399del
ENST00000493919.6:c.2020_2027del
ENST00000494123.6:c.5470_5477del
ENST00000497488.2:c.4582_4589del
ENST00000618469.2:c.5470_5477del
ENST00000634433.2:c.5347_5354del
ENST00000644379.2:c.5536_5543del
ENST00000644555.2:c.2020_2027del
ENST00000652672.2:c.5329_5336del
ENST00000484087.6:c.2032_2039del
ENST00000700081.1:n.1353_1360del
ENST00000700082.1:n.834_841del
ENST00000357654.9:c.5470_5477del
ENST00000471181.7:c.5533_5540del
ENST00000644379.1:c.1857_1864del
ENST00000352993.7:c.2044_2051del
ENST00000357654.7:c.5470_5477del
ENST00000461221.5:c.*5253_*5260del
ENST00000468300.5:c.2084_2091del
ENST00000471181.6:c.5533_5540del
ENST00000491747.6:c.2158_2165del
ENST00000493795.5:c.5329_5336del
ENST00000586385.5:c.400_407del
ENST00000591534.5:c.943_950del
ENST00000591849.5:c.169_176del
NM_007294.3:c.5470_5477del , LRG_292t1:c.5470_5477del
NM_007297.3:c.5329_5336del
NM_007298.3:c.2158_2165del
NM_007299.3:c.2084_2091del
NM_007300.3:c.5533_5540del
NR_027676.1:n.5606_5613del
NM_007294.4:c.5470_5477del
NM_007297.4:c.5329_5336del
NM_007299.4:c.2084_2091del
NM_007300.4:c.5533_5540del
NR_027676.2:n.5647_5654del