Canonical Allele Identifier: CA1327046217

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214730097_214730102delinsATATGG , CM000664.2:g.214730097_214730102delinsATATGG	GRCh38
NC_000002.11:g.215594821_215594826delinsATATGG , CM000664.1:g.215594821_215594826delinsATATGG	GRCh37
NC_000002.10:g.215303066_215303071delinsATATGG	NCBI36
NG_012047.2:g.84603_84608delinsCCATAT
NG_012047.3:g.84610_84615delinsCCATAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.2001+309_2001+314delinsCCATAT MANE Select	ENSP00000260947.4:n.2001+309_2001+314delinsCCATAT
ENST00000421162.2:c.648+309_648+314delinsCCATAT	ENSP00000392245.2:n.648+309_648+314delinsCCATAT
ENST00000613192.2:c.*64+309_*64+314delinsCCATAT	ENSP00000483275.2:n.*64+309_*64+314delinsCCATAT
ENST00000613374.5:c.591+309_591+314delinsCCATAT	ENSP00000484464.1:n.591+309_591+314delinsCCATAT
ENST00000613706.5:c.1593+309_1593+314delinsCCATAT	ENSP00000484976.2:n.1593+309_1593+314delinsCCATAT
ENST00000617164.5:c.1944+309_1944+314delinsCCATAT	ENSP00000480470.1:n.1944+309_1944+314delinsCCATAT
ENST00000619009.5:c.462+309_462+314delinsCCATAT	ENSP00000482293.1:n.462+309_462+314delinsCCATAT
ENST00000650978.1:c.3376+309_3376+314delinsCCATAT
ENST00000260947.8:c.2001+309_2001+314delinsCCATAT	ENSP00000260947.4:n.2001+309_2001+314delinsCCATAT
ENST00000432456.5:c.144+133_144+138delinsCCATAT
ENST00000455743.5:c.*1621+309_*1621+314delinsCCATAT	ENSP00000412186.1:n.*1621+309_*1621+314delinsCCATAT
ENST00000471590.5:n.336+309_336+314delinsCCATAT
ENST00000613192.1:c.171+309_171+314delinsCCATAT	ENSP00000483275.1:n.171+309_171+314delinsCCATAT
ENST00000613374.4:c.591+309_591+314delinsCCATAT	ENSP00000484464.1:n.591+309_591+314delinsCCATAT
ENST00000613706.4:c.648+309_648+314delinsCCATAT	ENSP00000484976.1:n.648+309_648+314delinsCCATAT
ENST00000617164.4:c.1944+309_1944+314delinsCCATAT	ENSP00000480470.1:n.1944+309_1944+314delinsCCATAT
ENST00000619009.4:c.462+309_462+314delinsCCATAT	ENSP00000482293.1:n.462+309_462+314delinsCCATAT
ENST00000620057.4:c.*667+309_*667+314delinsCCATAT	ENSP00000481988.1:n.*667+309_*667+314delinsCCATAT
NM_000465.3:c.2001+309_2001+314delinsCCATAT	NP_000456.2:n.2001+309_2001+314delinsCCATAT
NM_001282543.1:c.1944+309_1944+314delinsCCATAT	NP_001269472.1:n.1944+309_1944+314delinsCCATAT
NM_001282545.1:c.648+309_648+314delinsCCATAT	NP_001269474.1:n.648+309_648+314delinsCCATAT
NM_001282548.1:c.591+309_591+314delinsCCATAT	NP_001269477.1:n.591+309_591+314delinsCCATAT
NM_001282549.1:c.462+309_462+314delinsCCATAT	NP_001269478.1:n.462+309_462+314delinsCCATAT
NR_104212.1:n.1994+309_1994+314delinsCCATAT
NR_104215.1:n.1937+309_1937+314delinsCCATAT
NR_104216.1:n.1193+309_1193+314delinsCCATAT
XM_011511567.1:c.1947+309_1947+314delinsCCATAT	XP_011509869.1:n.1947+309_1947+314delinsCCATAT
XM_017004613.1:c.2100+309_2100+314delinsCCATAT	XP_016860102.1:n.2100+309_2100+314delinsCCATAT
XR_002959322.1:n.2367+133_2367+138delinsCCATAT
NM_000465.4:c.2001+309_2001+314delinsCCATAT MANE Select	NP_000456.2:n.2001+309_2001+314delinsCCATAT
NM_001282543.2:c.1944+309_1944+314delinsCCATAT	NP_001269472.1:n.1944+309_1944+314delinsCCATAT
NM_001282545.2:c.648+309_648+314delinsCCATAT	NP_001269474.1:n.648+309_648+314delinsCCATAT
NM_001282548.2:c.591+309_591+314delinsCCATAT	NP_001269477.1:n.591+309_591+314delinsCCATAT
NM_001282549.2:c.462+309_462+314delinsCCATAT	NP_001269478.1:n.462+309_462+314delinsCCATAT
NR_104212.2:n.1966+309_1966+314delinsCCATAT
NR_104215.2:n.1909+309_1909+314delinsCCATAT
NR_104216.2:n.1165+309_1165+314delinsCCATAT