Canonical Allele Identifier: CA658684094
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 495094
ClinVar RCV Id: RCV000585710
dbSNP Id: rs1555576921

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43057093_43057145dup , CM000679.2:g.43057093_43057145dup GRCh38
NC_000017.10:g.41209110_41209162dup , CM000679.1:g.41209110_41209162dup GRCh37
NC_000017.9:g.38462636_38462688dup NCBI36
NG_005905.2:g.160839_160891dup , LRG_292:g.160839_160891dup

Transcript Alleles

HGVS Amino-acid change
ENST00000461574.2:c.5191-10_5233dup
ENST00000470026.6:c.5194-10_5236dup
ENST00000473961.6:c.5068-10_5110dup
ENST00000476777.6:c.5188-10_5230dup
ENST00000477152.6:c.5116-10_5158dup
ENST00000478531.6:c.1882-10_1924dup
ENST00000489037.2:c.5116-10_5158dup
ENST00000493919.6:c.1744-10_1786dup
ENST00000494123.6:c.5194-10_5236dup
ENST00000497488.2:c.4306-10_4348dup
ENST00000618469.2:c.5194-10_5236dup
ENST00000634433.2:c.5071-10_5113dup
ENST00000644379.2:c.5260-10_5302dup
ENST00000644555.2:c.1744-10_1786dup
ENST00000652672.2:c.5053-10_5095dup
ENST00000484087.6:c.1756-10_1798dup
ENST00000357654.9:c.5194-10_5236dup
ENST00000471181.7:c.5257-10_5299dup
ENST00000644379.1:c.1581-10_1623dup
ENST00000352993.7:c.1768-10_1810dup
ENST00000357654.7:c.5194-10_5236dup
ENST00000461221.5:c.*4977-10_*5019dup
ENST00000468300.5:c.1882-10_1924dup
ENST00000471181.6:c.5257-10_5299dup
ENST00000491747.6:c.1882-10_1924dup
ENST00000493795.5:c.5053-10_5095dup
ENST00000586385.5:c.124-10_166dup
ENST00000591534.5:c.667-10_709dup
ENST00000591849.5:c.-98-6955_-98-6903dup ENSP00000465347.1:n.-98-6955_-98-6903dup
NM_007294.3:c.5194-10_5236dup , LRG_292t1:c.5194-10_5236dup
NM_007297.3:c.5053-10_5095dup
NM_007298.3:c.1882-10_1924dup
NM_007299.3:c.1882-10_1924dup
NM_007300.3:c.5257-10_5299dup
NR_027676.1:n.5330-10_5372dup
NM_007294.4:c.5194-10_5236dup
NM_007297.4:c.5053-10_5095dup
NM_007299.4:c.1882-10_1924dup
NM_007300.4:c.5257-10_5299dup
NR_027676.2:n.5371-10_5413dup