Canonical Allele Identifier: CA431136023

Gene: BARD1

Linked Data

• ClinVar Variation Id: 2121309
• ClinVar RCV Id: RCV003049094
• gnomAD v4: 2-214781403-A-T
• MyVariant Identifiers: chr2:g.215646127A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214781403A>T , CM000664.2:g.214781403A>T	GRCh38
NC_000002.11:g.215646127A>T , CM000664.1:g.215646127A>T	GRCh37
NC_000002.10:g.215354372A>T	NCBI36
NG_012047.2:g.33302T>A
NG_012047.3:g.33309T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.471T>A MANE Select	ENSP00000260947.4:p.Val157=
ENST00000421162.2:c.215+15658T>A	ENSP00000392245.2:n.215+15658T>A
ENST00000613192.2:c.158+28009T>A	ENSP00000483275.2:n.158+28009T>A
ENST00000613374.5:c.158+28009T>A	ENSP00000484464.1:n.158+28009T>A
ENST00000613706.5:c.471T>A	ENSP00000484976.2:p.Val157=
ENST00000617164.5:c.414T>A	ENSP00000480470.1:p.Val138=
ENST00000619009.5:c.364+10894T>A	ENSP00000482293.1:n.364+10894T>A
ENST00000650978.1:c.313T>A
ENST00000260947.8:c.471T>A	ENSP00000260947.4:p.Val157=
ENST00000421162.1:c.215+15658T>A	ENSP00000392245.1:n.215+15658T>A
ENST00000455743.5:c.*91T>A	ENSP00000412186.1:n.*91T>A
ENST00000471787.1:n.366T>A
ENST00000613192.1:c.73+28009T>A	ENSP00000483275.1:n.73+28009T>A
ENST00000613374.4:c.158+28009T>A	ENSP00000484464.1:n.158+28009T>A
ENST00000613706.4:c.215+15658T>A	ENSP00000484976.1:n.215+15658T>A
ENST00000617164.4:c.414T>A	ENSP00000480470.1:p.Val138=
ENST00000619009.4:c.364+10894T>A	ENSP00000482293.1:n.364+10894T>A
ENST00000620057.4:c.364+10894T>A	ENSP00000481988.1:n.364+10894T>A
NM_000465.3:c.471T>A	NP_000456.2:p.Val157=
NM_001282543.1:c.414T>A	NP_001269472.1:p.Val138=
NM_001282545.1:c.215+15658T>A	NP_001269474.1:n.215+15658T>A
NM_001282548.1:c.158+28009T>A	NP_001269477.1:n.158+28009T>A
NM_001282549.1:c.364+10894T>A	NP_001269478.1:n.364+10894T>A
NR_104212.1:n.464T>A
NR_104215.1:n.407T>A
NR_104216.1:n.506+10894T>A
XM_011511567.1:c.417T>A	XP_011509869.1:p.Val139=
XM_011511568.1:c.471T>A	XP_011509870.1:p.Val157=
XM_017004613.1:c.570T>A	XP_016860102.1:p.Val190=
XM_017004614.1:c.570T>A	XP_016860103.1:p.Val190=
XR_002959322.1:n.661T>A
NM_000465.4:c.471T>A MANE Select	NP_000456.2:p.Val157=
NM_001282543.2:c.414T>A	NP_001269472.1:p.Val138=
NM_001282545.2:c.215+15658T>A	NP_001269474.1:n.215+15658T>A
NM_001282548.2:c.158+28009T>A	NP_001269477.1:n.158+28009T>A
NM_001282549.2:c.364+10894T>A	NP_001269478.1:n.364+10894T>A
NR_104212.2:n.436T>A
NR_104215.2:n.379T>A
NR_104216.2:n.478+10894T>A