Canonical Allele Identifier: CA1327046389

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214730458_214730461delinsCATA , CM000664.2:g.214730458_214730461delinsCATA	GRCh38
NC_000002.11:g.215595182_215595185delinsCATA , CM000664.1:g.215595182_215595185delinsCATA	GRCh37
NC_000002.10:g.215303427_215303430delinsCATA	NCBI36
NG_012047.2:g.84244_84247delinsTATG
NG_012047.3:g.84251_84254delinsTATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1951_1954delinsTATG MANE Select	ENSP00000260947.4:p.Tyr651=
ENST00000421162.2:c.598_601delinsTATG	ENSP00000392245.2:p.Tyr200=
ENST00000613192.2:c.*14_*17delinsTATG	ENSP00000483275.2:n.*14_*17delinsTATG
ENST00000613374.5:c.541_544delinsTATG	ENSP00000484464.1:p.Tyr181=
ENST00000613706.5:c.1543_1546delinsTATG	ENSP00000484976.2:p.Tyr515=
ENST00000617164.5:c.1894_1897delinsTATG	ENSP00000480470.1:p.Tyr632=
ENST00000619009.5:c.412_415delinsTATG	ENSP00000482293.1:p.Tyr138=
ENST00000650978.1:c.3326_3329delinsTATG
ENST00000260947.8:c.1951_1954delinsTATG	ENSP00000260947.4:p.Tyr651=
ENST00000421162.1:c.598_601delinsTATG	ENSP00000392245.1:p.Tyr200=
ENST00000432456.5:c.48_51delinsTATG
ENST00000455743.5:c.*1571_*1574delinsTATG	ENSP00000412186.1:n.*1571_*1574delinsTATG
ENST00000471590.5:n.286_289delinsTATG
ENST00000613192.1:c.121_124delinsTATG	ENSP00000483275.1:p.Tyr41=
ENST00000613374.4:c.541_544delinsTATG	ENSP00000484464.1:p.Tyr181=
ENST00000613706.4:c.598_601delinsTATG	ENSP00000484976.1:p.Tyr200=
ENST00000617164.4:c.1894_1897delinsTATG	ENSP00000480470.1:p.Tyr632=
ENST00000619009.4:c.412_415delinsTATG	ENSP00000482293.1:p.Tyr138=
ENST00000620057.4:c.*617_*620delinsTATG	ENSP00000481988.1:n.*617_*620delinsTATG
NM_000465.3:c.1951_1954delinsTATG	NP_000456.2:p.Tyr651=
NM_001282543.1:c.1894_1897delinsTATG	NP_001269472.1:p.Tyr632=
NM_001282545.1:c.598_601delinsTATG	NP_001269474.1:p.Tyr200=
NM_001282548.1:c.541_544delinsTATG	NP_001269477.1:p.Tyr181=
NM_001282549.1:c.412_415delinsTATG	NP_001269478.1:p.Tyr138=
NR_104212.1:n.1944_1947delinsTATG
NR_104215.1:n.1887_1890delinsTATG
NR_104216.1:n.1143_1146delinsTATG
XM_011511567.1:c.1897_1900delinsTATG	XP_011509869.1:p.Tyr633=
XM_017004613.1:c.2050_2053delinsTATG	XP_016860102.1:p.Tyr684=
XR_002959322.1:n.2141_2144delinsTATG
NM_000465.4:c.1951_1954delinsTATG MANE Select	NP_000456.2:p.Tyr651=
NM_001282543.2:c.1894_1897delinsTATG	NP_001269472.1:p.Tyr632=
NM_001282545.2:c.598_601delinsTATG	NP_001269474.1:p.Tyr200=
NM_001282548.2:c.541_544delinsTATG	NP_001269477.1:p.Tyr181=
NM_001282549.2:c.412_415delinsTATG	NP_001269478.1:p.Tyr138=
NR_104212.2:n.1916_1919delinsTATG
NR_104215.2:n.1859_1862delinsTATG
NR_104216.2:n.1115_1118delinsTATG