Canonical Allele Identifier: CA1327046383

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214730453_214730460delinsAATTTCAT , CM000664.2:g.214730453_214730460delinsAATTTCAT	GRCh38
NC_000002.11:g.215595177_215595184delinsAATTTCAT , CM000664.1:g.215595177_215595184delinsAATTTCAT	GRCh37
NC_000002.10:g.215303422_215303429delinsAATTTCAT	NCBI36
NG_012047.2:g.84245_84252delinsATGAAATT
NG_012047.3:g.84252_84259delinsATGAAATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1952_1959delinsATGAAATT MANE Select	ENSP00000260947.4:p.Tyr651=
ENST00000421162.2:c.599_606delinsATGAAATT	ENSP00000392245.2:p.Tyr200=
ENST00000613192.2:c.*15_*22delinsATGAAATT	ENSP00000483275.2:n.*15_*22delinsATGAAATT
ENST00000613374.5:c.542_549delinsATGAAATT	ENSP00000484464.1:p.Tyr181=
ENST00000613706.5:c.1544_1551delinsATGAAATT	ENSP00000484976.2:p.Tyr515=
ENST00000617164.5:c.1895_1902delinsATGAAATT	ENSP00000480470.1:p.Tyr632=
ENST00000619009.5:c.413_420delinsATGAAATT	ENSP00000482293.1:p.Tyr138=
ENST00000650978.1:c.3327_3334delinsATGAAATT
ENST00000260947.8:c.1952_1959delinsATGAAATT	ENSP00000260947.4:p.Tyr651=
ENST00000421162.1:c.599_606delinsATGAAATT	ENSP00000392245.1:p.Tyr200=
ENST00000432456.5:c.49_56delinsATGAAATT
ENST00000455743.5:c.*1572_*1579delinsATGAAATT	ENSP00000412186.1:n.*1572_*1579delinsATGAAATT
ENST00000471590.5:n.287_294delinsATGAAATT
ENST00000613192.1:c.122_129delinsATGAAATT	ENSP00000483275.1:p.Tyr41=
ENST00000613374.4:c.542_549delinsATGAAATT	ENSP00000484464.1:p.Tyr181=
ENST00000613706.4:c.599_606delinsATGAAATT	ENSP00000484976.1:p.Tyr200=
ENST00000617164.4:c.1895_1902delinsATGAAATT	ENSP00000480470.1:p.Tyr632=
ENST00000619009.4:c.413_420delinsATGAAATT	ENSP00000482293.1:p.Tyr138=
ENST00000620057.4:c.*618_*625delinsATGAAATT	ENSP00000481988.1:n.*618_*625delinsATGAAATT
NM_000465.3:c.1952_1959delinsATGAAATT	NP_000456.2:p.Tyr651=
NM_001282543.1:c.1895_1902delinsATGAAATT	NP_001269472.1:p.Tyr632=
NM_001282545.1:c.599_606delinsATGAAATT	NP_001269474.1:p.Tyr200=
NM_001282548.1:c.542_549delinsATGAAATT	NP_001269477.1:p.Tyr181=
NM_001282549.1:c.413_420delinsATGAAATT	NP_001269478.1:p.Tyr138=
NR_104212.1:n.1945_1952delinsATGAAATT
NR_104215.1:n.1888_1895delinsATGAAATT
NR_104216.1:n.1144_1151delinsATGAAATT
XM_011511567.1:c.1898_1905delinsATGAAATT	XP_011509869.1:p.Tyr633=
XM_017004613.1:c.2051_2058delinsATGAAATT	XP_016860102.1:p.Tyr684=
XR_002959322.1:n.2142_2149delinsATGAAATT
NM_000465.4:c.1952_1959delinsATGAAATT MANE Select	NP_000456.2:p.Tyr651=
NM_001282543.2:c.1895_1902delinsATGAAATT	NP_001269472.1:p.Tyr632=
NM_001282545.2:c.599_606delinsATGAAATT	NP_001269474.1:p.Tyr200=
NM_001282548.2:c.542_549delinsATGAAATT	NP_001269477.1:p.Tyr181=
NM_001282549.2:c.413_420delinsATGAAATT	NP_001269478.1:p.Tyr138=
NR_104212.2:n.1917_1924delinsATGAAATT
NR_104215.2:n.1860_1867delinsATGAAATT
NR_104216.2:n.1116_1123delinsATGAAATT