Canonical Allele Identifier: CA2090173

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214745742T>C , CM000664.2:g.214745742T>C	GRCh38
NC_000002.11:g.215610466T>C , CM000664.1:g.215610466T>C	GRCh37
NC_000002.10:g.215318711T>C	NCBI36
NG_012047.2:g.68963A>G
NG_012047.3:g.68970A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000465.4:c.1790A>G MANE Select	NP_000456.2:p.Tyr597Cys
ENST00000260947.9:c.1790A>G MANE Select	ENSP00000260947.4:p.Tyr597Cys
NM_000465.3:c.1790A>G	NP_000456.2:p.Tyr597Cys
NM_001282543.1:c.1733A>G	NP_001269472.1:p.Tyr578Cys
NM_001282543.2:c.1733A>G	NP_001269472.1:p.Tyr578Cys
NM_001282545.1:c.437A>G	NP_001269474.1:p.Tyr146Cys
NM_001282545.2:c.437A>G	NP_001269474.1:p.Tyr146Cys
NM_001282548.1:c.380A>G	NP_001269477.1:p.Tyr127Cys
NM_001282548.2:c.380A>G	NP_001269477.1:p.Tyr127Cys
NM_001282549.1:c.365-15234A>G	NP_001269478.1:n.365-15234A>G
NM_001282549.2:c.365-15234A>G	NP_001269478.1:n.365-15234A>G
NR_104212.1:n.1783A>G
NR_104212.2:n.1755A>G
NR_104215.1:n.1726A>G
NR_104215.2:n.1698A>G
NR_104216.1:n.982A>G
NR_104216.2:n.954A>G
ENST00000260947.8:c.1790A>G	ENSP00000260947.4:p.Tyr597Cys
ENST00000421162.1:c.437A>G	ENSP00000392245.1:p.Tyr146Cys
ENST00000421162.2:c.437A>G	ENSP00000392245.2:p.Tyr146Cys
ENST00000455743.5:c.*1410A>G	ENSP00000412186.1:n.*1410A>G
ENST00000465841.1:n.145A>G
ENST00000613192.1:c.74-15234A>G	ENSP00000483275.1:n.74-15234A>G
ENST00000613192.2:c.159-15234A>G	ENSP00000483275.2:n.159-15234A>G
ENST00000613374.4:c.380A>G	ENSP00000484464.1:p.Tyr127Cys
ENST00000613374.5:c.380A>G	ENSP00000484464.1:p.Tyr127Cys
ENST00000613706.4:c.437A>G	ENSP00000484976.1:p.Tyr146Cys
ENST00000613706.5:c.1382A>G	ENSP00000484976.2:p.Tyr461Cys
ENST00000617164.4:c.1733A>G	ENSP00000480470.1:p.Tyr578Cys
ENST00000617164.5:c.1733A>G	ENSP00000480470.1:p.Tyr578Cys
ENST00000619009.4:c.365-15234A>G	ENSP00000482293.1:n.365-15234A>G
ENST00000619009.5:c.365-15234A>G	ENSP00000482293.1:n.365-15234A>G
ENST00000620057.4:c.*456A>G	ENSP00000481988.1:n.*456A>G
ENST00000650978.1:c.3165A>G
XM_011511567.1:c.1736A>G	XP_011509869.1:p.Tyr579Cys
XM_011511568.1:c.1790A>G	XP_011509870.1:p.Tyr597Cys
XM_017004613.1:c.1889A>G	XP_016860102.1:p.Tyr630Cys
XM_017004614.1:c.1889A>G	XP_016860103.1:p.Tyr630Cys
XR_002959322.1:n.1980A>G