Canonical Allele Identifier: CA1327045103
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214728030_214728031delinsAT , CM000664.2:g.214728030_214728031delinsAT GRCh38
NC_000002.11:g.215592754_215592755delinsAT , CM000664.1:g.215592754_215592755delinsAT GRCh37
NC_000002.10:g.215300999_215301000delinsAT NCBI36
NG_012047.2:g.86674_86675delinsAT
NG_012047.3:g.86681_86682delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000260947.9:c.*645_*646delinsAT MANE Select ENSP00000260947.4:n.*645_*646delinsAT
ENST00000260947.8:c.*645_*646delinsAT ENSP00000260947.4:n.*645_*646delinsAT
ENST00000613374.4:c.*645_*646delinsAT ENSP00000484464.1:n.*645_*646delinsAT
ENST00000613706.4:c.*645_*646delinsAT ENSP00000484976.1:n.*645_*646delinsAT
ENST00000617164.4:c.*645_*646delinsAT ENSP00000480470.1:n.*645_*646delinsAT
ENST00000619009.4:c.*645_*646delinsAT ENSP00000482293.1:n.*645_*646delinsAT
NM_000465.3:c.*645_*646delinsAT NP_000456.2:n.*645_*646delinsAT
NM_001282543.1:c.*645_*646delinsAT NP_001269472.1:n.*645_*646delinsAT
NM_001282545.1:c.*645_*646delinsAT NP_001269474.1:n.*645_*646delinsAT
NM_001282548.1:c.*645_*646delinsAT NP_001269477.1:n.*645_*646delinsAT
NM_001282549.1:c.*645_*646delinsAT NP_001269478.1:n.*645_*646delinsAT
NR_104212.1:n.2972_2973delinsAT
NR_104215.1:n.2915_2916delinsAT
NR_104216.1:n.2171_2172delinsAT
XM_011511567.1:c.*645_*646delinsAT XP_011509869.1:n.*645_*646delinsAT
XM_017004613.1:c.*645_*646delinsAT XP_016860102.1:n.*645_*646delinsAT
NM_000465.4:c.*645_*646delinsAT MANE Select NP_000456.2:n.*645_*646delinsAT
NM_001282543.2:c.*645_*646delinsAT NP_001269472.1:n.*645_*646delinsAT
NM_001282545.2:c.*645_*646delinsAT NP_001269474.1:n.*645_*646delinsAT
NM_001282548.2:c.*645_*646delinsAT NP_001269477.1:n.*645_*646delinsAT
NM_001282549.2:c.*645_*646delinsAT NP_001269478.1:n.*645_*646delinsAT
NR_104212.2:n.2944_2945delinsAT
NR_104215.2:n.2887_2888delinsAT
NR_104216.2:n.2143_2144delinsAT