Canonical Allele Identifier: CA2582342122

Gene: BARD1

Linked Data

• ClinVar Variation Id: 2583626
• ClinVar RCV Id: RCV003334548 ; RCV004334132

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214809404_214809412del , CM000664.2:g.214809404_214809412del	GRCh38
NC_000002.11:g.215674128_215674136del , CM000664.1:g.215674128_215674136del	GRCh37
NC_000002.10:g.215382373_215382381del	NCBI36
NG_012047.2:g.5295_5303del
NG_012047.3:g.5302_5310del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.158+2_158+10del
ENST00000421162.2:c.158+2_158+10del
ENST00000613192.2:c.158+2_158+10del
ENST00000613374.5:c.158+2_158+10del
ENST00000613706.5:c.158+2_158+10del
ENST00000617164.5:c.158+2_158+10del
ENST00000619009.5:c.158+2_158+10del
ENST00000260947.8:c.158+2_158+10del
ENST00000421162.1:c.158+2_158+10del
ENST00000455743.5:c.158+2_158+10del
ENST00000471787.1:n.259+2_259+10del
ENST00000479904.1:n.249+2_249+10del
ENST00000613192.1:c.73+2_73+10del
ENST00000613374.4:c.158+2_158+10del
ENST00000613706.4:c.158+2_158+10del
ENST00000617164.4:c.158+2_158+10del
ENST00000619009.4:c.158+2_158+10del
ENST00000620057.4:c.158+2_158+10del
NM_000465.3:c.158+2_158+10del
NM_001282543.1:c.158+2_158+10del
NM_001282545.1:c.158+2_158+10del
NM_001282548.1:c.158+2_158+10del
NM_001282549.1:c.158+2_158+10del
NR_104212.1:n.300+2_300+10del
NR_104215.1:n.300+2_300+10del
NR_104216.1:n.300+2_300+10del
XM_011511568.1:c.158+2_158+10del
XM_017004613.1:c.158+2_158+10del
XM_017004614.1:c.158+2_158+10del
XR_002959322.1:n.249+2_249+10del
NM_000465.4:c.158+2_158+10del
NM_001282543.2:c.158+2_158+10del
NM_001282545.2:c.158+2_158+10del
NM_001282548.2:c.158+2_158+10del
NM_001282549.2:c.158+2_158+10del
NR_104212.2:n.272+2_272+10del
NR_104215.2:n.272+2_272+10del
NR_104216.2:n.272+2_272+10del