Canonical Allele Identifier: CA1327046396
Gene: BARD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214730466_214730467delinsTC , CM000664.2:g.214730466_214730467delinsTC GRCh38
NC_000002.11:g.215595190_215595191delinsTC , CM000664.1:g.215595190_215595191delinsTC GRCh37
NC_000002.10:g.215303435_215303436delinsTC NCBI36
NG_012047.2:g.84238_84239delinsGA
NG_012047.3:g.84245_84246delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000260947.9:c.1945_1946delinsGA MANE Select ENSP00000260947.4:p.Glu649=
ENST00000421162.2:c.592_593delinsGA ENSP00000392245.2:p.Glu198=
ENST00000613192.2:c.*8_*9delinsGA ENSP00000483275.2:n.*8_*9delinsGA
ENST00000613374.5:c.535_536delinsGA ENSP00000484464.1:p.Glu179=
ENST00000613706.5:c.1537_1538delinsGA ENSP00000484976.2:p.Glu513=
ENST00000617164.5:c.1888_1889delinsGA ENSP00000480470.1:p.Glu630=
ENST00000619009.5:c.406_407delinsGA ENSP00000482293.1:p.Glu136=
ENST00000650978.1:c.3320_3321delinsGA
ENST00000260947.8:c.1945_1946delinsGA ENSP00000260947.4:p.Glu649=
ENST00000421162.1:c.592_593delinsGA ENSP00000392245.1:p.Glu198=
ENST00000432456.5:c.42_43delinsGA
ENST00000455743.5:c.*1565_*1566delinsGA ENSP00000412186.1:n.*1565_*1566delinsGA
ENST00000471590.5:n.280_281delinsGA
ENST00000613192.1:c.115_116delinsGA ENSP00000483275.1:p.Glu39=
ENST00000613374.4:c.535_536delinsGA ENSP00000484464.1:p.Glu179=
ENST00000613706.4:c.592_593delinsGA ENSP00000484976.1:p.Glu198=
ENST00000617164.4:c.1888_1889delinsGA ENSP00000480470.1:p.Glu630=
ENST00000619009.4:c.406_407delinsGA ENSP00000482293.1:p.Glu136=
ENST00000620057.4:c.*611_*612delinsGA ENSP00000481988.1:n.*611_*612delinsGA
NM_000465.3:c.1945_1946delinsGA NP_000456.2:p.Glu649=
NM_001282543.1:c.1888_1889delinsGA NP_001269472.1:p.Glu630=
NM_001282545.1:c.592_593delinsGA NP_001269474.1:p.Glu198=
NM_001282548.1:c.535_536delinsGA NP_001269477.1:p.Glu179=
NM_001282549.1:c.406_407delinsGA NP_001269478.1:p.Glu136=
NR_104212.1:n.1938_1939delinsGA
NR_104215.1:n.1881_1882delinsGA
NR_104216.1:n.1137_1138delinsGA
XM_011511567.1:c.1891_1892delinsGA XP_011509869.1:p.Glu631=
XM_017004613.1:c.2044_2045delinsGA XP_016860102.1:p.Glu682=
XR_002959322.1:n.2135_2136delinsGA
NM_000465.4:c.1945_1946delinsGA MANE Select NP_000456.2:p.Glu649=
NM_001282543.2:c.1888_1889delinsGA NP_001269472.1:p.Glu630=
NM_001282545.2:c.592_593delinsGA NP_001269474.1:p.Glu198=
NM_001282548.2:c.535_536delinsGA NP_001269477.1:p.Glu179=
NM_001282549.2:c.406_407delinsGA NP_001269478.1:p.Glu136=
NR_104212.2:n.1910_1911delinsGA
NR_104215.2:n.1853_1854delinsGA
NR_104216.2:n.1109_1110delinsGA