Canonical Allele Identifier: CA431136374

Gene: BARD1

Linked Data

• ClinVar Variation Id: 1332127
• ClinVar RCV Id: RCV001804643 ; RCV001869527
• dbSNP Id: rs1695029571
• MyVariant Identifiers: chr2:g.215646169A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214781445A>T , CM000664.2:g.214781445A>T	GRCh38
NC_000002.11:g.215646169A>T , CM000664.1:g.215646169A>T	GRCh37
NC_000002.10:g.215354414A>T	NCBI36
NG_012047.2:g.33260T>A
NG_012047.3:g.33267T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.429T>A MANE Select	ENSP00000260947.4:p.Ile143=
ENST00000421162.2:c.215+15616T>A	ENSP00000392245.2:n.215+15616T>A
ENST00000613192.2:c.158+27967T>A	ENSP00000483275.2:n.158+27967T>A
ENST00000613374.5:c.158+27967T>A	ENSP00000484464.1:n.158+27967T>A
ENST00000613706.5:c.429T>A	ENSP00000484976.2:p.Ile143=
ENST00000617164.5:c.372T>A	ENSP00000480470.1:p.Ile124=
ENST00000619009.5:c.364+10852T>A	ENSP00000482293.1:n.364+10852T>A
ENST00000650978.1:c.271T>A
ENST00000260947.8:c.429T>A	ENSP00000260947.4:p.Ile143=
ENST00000421162.1:c.215+15616T>A	ENSP00000392245.1:n.215+15616T>A
ENST00000455743.5:c.*49T>A	ENSP00000412186.1:n.*49T>A
ENST00000471787.1:n.324T>A
ENST00000613192.1:c.73+27967T>A	ENSP00000483275.1:n.73+27967T>A
ENST00000613374.4:c.158+27967T>A	ENSP00000484464.1:n.158+27967T>A
ENST00000613706.4:c.215+15616T>A	ENSP00000484976.1:n.215+15616T>A
ENST00000617164.4:c.372T>A	ENSP00000480470.1:p.Ile124=
ENST00000619009.4:c.364+10852T>A	ENSP00000482293.1:n.364+10852T>A
ENST00000620057.4:c.364+10852T>A	ENSP00000481988.1:n.364+10852T>A
NM_000465.3:c.429T>A	NP_000456.2:p.Ile143=
NM_001282543.1:c.372T>A	NP_001269472.1:p.Ile124=
NM_001282545.1:c.215+15616T>A	NP_001269474.1:n.215+15616T>A
NM_001282548.1:c.158+27967T>A	NP_001269477.1:n.158+27967T>A
NM_001282549.1:c.364+10852T>A	NP_001269478.1:n.364+10852T>A
NR_104212.1:n.422T>A
NR_104215.1:n.365T>A
NR_104216.1:n.506+10852T>A
XM_011511567.1:c.375T>A	XP_011509869.1:p.Ile125=
XM_011511568.1:c.429T>A	XP_011509870.1:p.Ile143=
XM_017004613.1:c.528T>A	XP_016860102.1:p.Ile176=
XM_017004614.1:c.528T>A	XP_016860103.1:p.Ile176=
XR_002959322.1:n.619T>A
NM_000465.4:c.429T>A MANE Select	NP_000456.2:p.Ile143=
NM_001282543.2:c.372T>A	NP_001269472.1:p.Ile124=
NM_001282545.2:c.215+15616T>A	NP_001269474.1:n.215+15616T>A
NM_001282548.2:c.158+27967T>A	NP_001269477.1:n.158+27967T>A
NM_001282549.2:c.364+10852T>A	NP_001269478.1:n.364+10852T>A
NR_104212.2:n.394T>A
NR_104215.2:n.337T>A
NR_104216.2:n.478+10852T>A