Canonical Allele Identifier: CA2499215623
Gene: BARD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1050223
ClinVar RCV Id: RCV001357314
dbSNP Id: rs2106038518

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214752445_214752556del , CM000664.2:g.214752445_214752556del GRCh38
NC_000002.11:g.215617169_215617280del , CM000664.1:g.215617169_215617280del GRCh37
NC_000002.10:g.215325414_215325525del NCBI36
NG_012047.2:g.62149_62260del
NG_012047.3:g.62156_62267del

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.1569-1_1677+2del
ENST00000421162.2:c.216-1_324+2del
ENST00000613192.2:c.159-22048_159-21937del ENSP00000483275.2:n.159-22048_159-21937de...
ENST00000613374.5:c.159-1_267+2del
ENST00000613706.5:c.1161-1_1269+2del
ENST00000617164.5:c.1512-1_1620+2del
ENST00000619009.5:c.365-22048_365-21937del ENSP00000482293.1:n.365-22048_365-21937de...
ENST00000650978.1:c.2944-1_3052+2del
ENST00000260947.8:c.1569-1_1677+2del
ENST00000421162.1:c.216-1_324+2del
ENST00000455743.5:c.*1189-1_*1297+2del
ENST00000613192.1:c.74-22048_74-21937del ENSP00000483275.1:n.74-22048_74-21937del
ENST00000613374.4:c.159-1_267+2del
ENST00000613706.4:c.216-1_324+2del
ENST00000617164.4:c.1512-1_1620+2del
ENST00000619009.4:c.365-22048_365-21937del ENSP00000482293.1:n.365-22048_365-21937de...
ENST00000620057.4:c.*235-1_*343+2del
NM_000465.3:c.1569-1_1677+2del
NM_001282543.1:c.1512-1_1620+2del
NM_001282545.1:c.216-1_324+2del
NM_001282548.1:c.159-1_267+2del
NM_001282549.1:c.365-22048_365-21937del NP_001269478.1:n.365-22048_365-21937del
NR_104212.1:n.1562-1_1670+2del
NR_104215.1:n.1505-1_1613+2del
NR_104216.1:n.761-1_869+2del
XM_011511567.1:c.1515-1_1623+2del
XM_011511568.1:c.1569-1_1677+2del
XM_017004613.1:c.1668-1_1776+2del
XM_017004614.1:c.1668-1_1776+2del
XR_002959322.1:n.1759-1_1867+2del
NM_000465.4:c.1569-1_1677+2del
NM_001282543.2:c.1512-1_1620+2del
NM_001282545.2:c.216-1_324+2del
NM_001282548.2:c.159-1_267+2del
NM_001282549.2:c.365-22048_365-21937del NP_001269478.1:n.365-22048_365-21937del
NR_104212.2:n.1534-1_1642+2del
NR_104215.2:n.1477-1_1585+2del
NR_104216.2:n.733-1_841+2del