Canonical Allele Identifier: CA1327045407
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214728630_214728634delinsCACAA , CM000664.2:g.214728630_214728634delinsCACAA GRCh38
NC_000002.11:g.215593354_215593358delinsCACAA , CM000664.1:g.215593354_215593358delinsCACAA GRCh37
NC_000002.10:g.215301599_215301603delinsCACAA NCBI36
NG_012047.2:g.86071_86075delinsTTGTG
NG_012047.3:g.86078_86082delinsTTGTG

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.*42_*46delinsTTGTG MANE Select ENSP00000260947.4:n.*42_*46delinsTTGTG
ENST00000613374.5:c.*42_*46delinsTTGTG ENSP00000484464.1:n.*42_*46delinsTTGTG
ENST00000613706.5:c.*42_*46delinsTTGTG ENSP00000484976.2:n.*42_*46delinsTTGTG
ENST00000617164.5:c.*42_*46delinsTTGTG ENSP00000480470.1:n.*42_*46delinsTTGTG
ENST00000619009.5:c.*42_*46delinsTTGTG ENSP00000482293.1:n.*42_*46delinsTTGTG
ENST00000650978.1:c.3751_3755delinsTTGTG
ENST00000260947.8:c.*42_*46delinsTTGTG ENSP00000260947.4:n.*42_*46delinsTTGTG
ENST00000432456.5:c.519_523delinsTTGTG
ENST00000471590.5:n.711_715delinsTTGTG
ENST00000613374.4:c.*42_*46delinsTTGTG ENSP00000484464.1:n.*42_*46delinsTTGTG
ENST00000613706.4:c.*42_*46delinsTTGTG ENSP00000484976.1:n.*42_*46delinsTTGTG
ENST00000617164.4:c.*42_*46delinsTTGTG ENSP00000480470.1:n.*42_*46delinsTTGTG
ENST00000619009.4:c.*42_*46delinsTTGTG ENSP00000482293.1:n.*42_*46delinsTTGTG
NM_000465.3:c.*42_*46delinsTTGTG NP_000456.2:n.*42_*46delinsTTGTG
NM_001282543.1:c.*42_*46delinsTTGTG NP_001269472.1:n.*42_*46delinsTTGTG
NM_001282545.1:c.*42_*46delinsTTGTG NP_001269474.1:n.*42_*46delinsTTGTG
NM_001282548.1:c.*42_*46delinsTTGTG NP_001269477.1:n.*42_*46delinsTTGTG
NM_001282549.1:c.*42_*46delinsTTGTG NP_001269478.1:n.*42_*46delinsTTGTG
NR_104212.1:n.2369_2373delinsTTGTG
NR_104215.1:n.2312_2316delinsTTGTG
NR_104216.1:n.1568_1572delinsTTGTG
XM_011511567.1:c.*42_*46delinsTTGTG XP_011509869.1:n.*42_*46delinsTTGTG
XM_017004613.1:c.*42_*46delinsTTGTG XP_016860102.1:n.*42_*46delinsTTGTG
XR_002959322.1:n.2742_2746delinsTTGTG
NM_000465.4:c.*42_*46delinsTTGTG MANE Select NP_000456.2:n.*42_*46delinsTTGTG
NM_001282543.2:c.*42_*46delinsTTGTG NP_001269472.1:n.*42_*46delinsTTGTG
NM_001282545.2:c.*42_*46delinsTTGTG NP_001269474.1:n.*42_*46delinsTTGTG
NM_001282548.2:c.*42_*46delinsTTGTG NP_001269477.1:n.*42_*46delinsTTGTG
NM_001282549.2:c.*42_*46delinsTTGTG NP_001269478.1:n.*42_*46delinsTTGTG
NR_104212.2:n.2341_2345delinsTTGTG
NR_104215.2:n.2284_2288delinsTTGTG
NR_104216.2:n.1540_1544delinsTTGTG