Canonical Allele Identifier: CA431392004

Gene: BARD1

Linked Data

• ClinVar Variation Id: 1763027
• ClinVar RCV Id: RCV003103495 ; RCV002434695
• MyVariant Identifiers: chr2:g.215645764G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214781040G>C , CM000664.2:g.214781040G>C	GRCh38
NC_000002.11:g.215645764G>C , CM000664.1:g.215645764G>C	GRCh37
NC_000002.10:g.215354009G>C	NCBI36
NG_012047.2:g.33665C>G
NG_012047.3:g.33672C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.834C>G MANE Select	ENSP00000260947.4:p.Val278=
ENST00000421162.2:c.215+16021C>G	ENSP00000392245.2:n.215+16021C>G
ENST00000613192.2:c.158+28372C>G	ENSP00000483275.2:n.158+28372C>G
ENST00000613374.5:c.158+28372C>G	ENSP00000484464.1:n.158+28372C>G
ENST00000613706.5:c.834C>G	ENSP00000484976.2:p.Val278=
ENST00000617164.5:c.777C>G	ENSP00000480470.1:p.Val259=
ENST00000619009.5:c.364+11257C>G	ENSP00000482293.1:n.364+11257C>G
ENST00000650978.1:c.676C>G
ENST00000260947.8:c.834C>G	ENSP00000260947.4:p.Val278=
ENST00000421162.1:c.215+16021C>G	ENSP00000392245.1:n.215+16021C>G
ENST00000455743.5:c.*454C>G	ENSP00000412186.1:n.*454C>G
ENST00000471787.1:n.729C>G
ENST00000613192.1:c.73+28372C>G	ENSP00000483275.1:n.73+28372C>G
ENST00000613374.4:c.158+28372C>G	ENSP00000484464.1:n.158+28372C>G
ENST00000613706.4:c.215+16021C>G	ENSP00000484976.1:n.215+16021C>G
ENST00000617164.4:c.777C>G	ENSP00000480470.1:p.Val259=
ENST00000619009.4:c.364+11257C>G	ENSP00000482293.1:n.364+11257C>G
ENST00000620057.4:c.364+11257C>G	ENSP00000481988.1:n.364+11257C>G
NM_000465.3:c.834C>G	NP_000456.2:p.Val278=
NM_001282543.1:c.777C>G	NP_001269472.1:p.Val259=
NM_001282545.1:c.215+16021C>G	NP_001269474.1:n.215+16021C>G
NM_001282548.1:c.158+28372C>G	NP_001269477.1:n.158+28372C>G
NM_001282549.1:c.364+11257C>G	NP_001269478.1:n.364+11257C>G
NR_104212.1:n.827C>G
NR_104215.1:n.770C>G
NR_104216.1:n.506+11257C>G
XM_011511567.1:c.780C>G	XP_011509869.1:p.Val260=
XM_011511568.1:c.834C>G	XP_011509870.1:p.Val278=
XM_017004613.1:c.933C>G	XP_016860102.1:p.Val311=
XM_017004614.1:c.933C>G	XP_016860103.1:p.Val311=
XR_002959322.1:n.1024C>G
NM_000465.4:c.834C>G MANE Select	NP_000456.2:p.Val278=
NM_001282543.2:c.777C>G	NP_001269472.1:p.Val259=
NM_001282545.2:c.215+16021C>G	NP_001269474.1:n.215+16021C>G
NM_001282548.2:c.158+28372C>G	NP_001269477.1:n.158+28372C>G
NM_001282549.2:c.364+11257C>G	NP_001269478.1:n.364+11257C>G
NR_104212.2:n.799C>G
NR_104215.2:n.742C>G
NR_104216.2:n.478+11257C>G