Canonical Allele Identifier: CA2582342055
Gene: BARD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2583698
ClinVar RCV Id: RCV003334620

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214730336_214730500del , CM000664.2:g.214730336_214730500del GRCh38
NC_000002.11:g.215595060_215595224del , CM000664.1:g.215595060_215595224del GRCh37
NC_000002.10:g.215303305_215303469del NCBI36
NG_012047.2:g.84207_84371del
NG_012047.3:g.84214_84378del

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.1914_2001+77del
ENST00000421162.2:c.561_648+77del
ENST00000613192.2:c.169_*64+77del
ENST00000613374.5:c.504_591+77del
ENST00000613706.5:c.1506_1593+77del
ENST00000617164.5:c.1857_1944+77del
ENST00000619009.5:c.375_462+77del
ENST00000650978.1:c.3289_3376+77del
ENST00000260947.8:c.1914_2001+77del
ENST00000432456.5:c.11_99-54del
ENST00000455743.5:c.*1534_*1621+77del
ENST00000471590.5:n.249_336+77del
ENST00000613192.1:c.84_171+77del
ENST00000613374.4:c.504_591+77del
ENST00000613706.4:c.561_648+77del
ENST00000617164.4:c.1857_1944+77del
ENST00000619009.4:c.375_462+77del
ENST00000620057.4:c.*580_*667+77del
NM_000465.3:c.1914_2001+77del
NM_001282543.1:c.1857_1944+77del
NM_001282545.1:c.561_648+77del
NM_001282548.1:c.504_591+77del
NM_001282549.1:c.375_462+77del
NR_104212.1:n.1907_1994+77del
NR_104215.1:n.1850_1937+77del
NR_104216.1:n.1106_1193+77del
XM_011511567.1:c.1860_1947+77del
XM_017004613.1:c.2013_2100+77del
XR_002959322.1:n.2104_2268del
NM_000465.4:c.1914_2001+77del
NM_001282543.2:c.1857_1944+77del
NM_001282545.2:c.561_648+77del
NM_001282548.2:c.504_591+77del
NM_001282549.2:c.375_462+77del
NR_104212.2:n.1879_1966+77del
NR_104215.2:n.1822_1909+77del
NR_104216.2:n.1078_1165+77del