Canonical Allele Identifier: CA169829

Gene: BARD1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214781293C>T , CM000664.2:g.214781293C>T	GRCh38
NC_000002.11:g.215646017C>T , CM000664.1:g.215646017C>T	GRCh37
NC_000002.10:g.215354262C>T	NCBI36
NG_012047.2:g.33412G>A
NG_012047.3:g.33419G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.581G>A MANE Select	ENSP00000260947.4:p.Arg194Lys
ENST00000421162.2:c.215+15768G>A	ENSP00000392245.2:n.215+15768G>A
ENST00000613192.2:c.158+28119G>A	ENSP00000483275.2:n.158+28119G>A
ENST00000613374.5:c.158+28119G>A	ENSP00000484464.1:n.158+28119G>A
ENST00000613706.5:c.581G>A	ENSP00000484976.2:p.Arg194Lys
ENST00000617164.5:c.524G>A	ENSP00000480470.1:p.Arg175Lys
ENST00000619009.5:c.364+11004G>A	ENSP00000482293.1:n.364+11004G>A
ENST00000650978.1:c.423G>A
ENST00000260947.8:c.581G>A	ENSP00000260947.4:p.Arg194Lys
ENST00000421162.1:c.215+15768G>A	ENSP00000392245.1:n.215+15768G>A
ENST00000455743.5:c.*201G>A	ENSP00000412186.1:n.*201G>A
ENST00000471787.1:n.476G>A
ENST00000613192.1:c.73+28119G>A	ENSP00000483275.1:n.73+28119G>A
ENST00000613374.4:c.158+28119G>A	ENSP00000484464.1:n.158+28119G>A
ENST00000613706.4:c.215+15768G>A	ENSP00000484976.1:n.215+15768G>A
ENST00000617164.4:c.524G>A	ENSP00000480470.1:p.Arg175Lys
ENST00000619009.4:c.364+11004G>A	ENSP00000482293.1:n.364+11004G>A
ENST00000620057.4:c.364+11004G>A	ENSP00000481988.1:n.364+11004G>A
NM_000465.3:c.581G>A	NP_000456.2:p.Arg194Lys
NM_001282543.1:c.524G>A	NP_001269472.1:p.Arg175Lys
NM_001282545.1:c.215+15768G>A	NP_001269474.1:n.215+15768G>A
NM_001282548.1:c.158+28119G>A	NP_001269477.1:n.158+28119G>A
NM_001282549.1:c.364+11004G>A	NP_001269478.1:n.364+11004G>A
NR_104212.1:n.574G>A
NR_104215.1:n.517G>A
NR_104216.1:n.506+11004G>A
XM_011511567.1:c.527G>A	XP_011509869.1:p.Arg176Lys
XM_011511568.1:c.581G>A	XP_011509870.1:p.Arg194Lys
XM_017004613.1:c.680G>A	XP_016860102.1:p.Arg227Lys
XM_017004614.1:c.680G>A	XP_016860103.1:p.Arg227Lys
XR_002959322.1:n.771G>A
NM_000465.4:c.581G>A MANE Select	NP_000456.2:p.Arg194Lys
NM_001282543.2:c.524G>A	NP_001269472.1:p.Arg175Lys
NM_001282545.2:c.215+15768G>A	NP_001269474.1:n.215+15768G>A
NM_001282548.2:c.158+28119G>A	NP_001269477.1:n.158+28119G>A
NM_001282549.2:c.364+11004G>A	NP_001269478.1:n.364+11004G>A
NR_104212.2:n.546G>A
NR_104215.2:n.489G>A
NR_104216.2:n.478+11004G>A