Canonical Allele Identifier: CA350457722

Gene: BARD1

Linked Data

• ClinVar Variation Id: 824912
• ClinVar RCV Id: RCV001022530
• dbSNP Id: rs1574821459
• MyVariant Identifiers: chr2:g.215646152G>C (hg19) ; chr2:g.214781428G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214781428G>C , CM000664.2:g.214781428G>C	GRCh38
NC_000002.11:g.215646152G>C , CM000664.1:g.215646152G>C	GRCh37
NC_000002.10:g.215354397G>C	NCBI36
NG_012047.2:g.33277C>G
NG_012047.3:g.33284C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.446C>G MANE Select	ENSP00000260947.4:p.Pro149Arg
ENST00000421162.2:c.215+15633C>G	ENSP00000392245.2:n.215+15633C>G
ENST00000613192.2:c.158+27984C>G	ENSP00000483275.2:n.158+27984C>G
ENST00000613374.5:c.158+27984C>G	ENSP00000484464.1:n.158+27984C>G
ENST00000613706.5:c.446C>G	ENSP00000484976.2:p.Pro149Arg
ENST00000617164.5:c.389C>G	ENSP00000480470.1:p.Pro130Arg
ENST00000619009.5:c.364+10869C>G	ENSP00000482293.1:n.364+10869C>G
ENST00000650978.1:c.288C>G
ENST00000260947.8:c.446C>G	ENSP00000260947.4:p.Pro149Arg
ENST00000421162.1:c.215+15633C>G	ENSP00000392245.1:n.215+15633C>G
ENST00000455743.5:c.*66C>G	ENSP00000412186.1:n.*66C>G
ENST00000471787.1:n.341C>G
ENST00000613192.1:c.73+27984C>G	ENSP00000483275.1:n.73+27984C>G
ENST00000613374.4:c.158+27984C>G	ENSP00000484464.1:n.158+27984C>G
ENST00000613706.4:c.215+15633C>G	ENSP00000484976.1:n.215+15633C>G
ENST00000617164.4:c.389C>G	ENSP00000480470.1:p.Pro130Arg
ENST00000619009.4:c.364+10869C>G	ENSP00000482293.1:n.364+10869C>G
ENST00000620057.4:c.364+10869C>G	ENSP00000481988.1:n.364+10869C>G
NM_000465.3:c.446C>G	NP_000456.2:p.Pro149Arg
NM_001282543.1:c.389C>G	NP_001269472.1:p.Pro130Arg
NM_001282545.1:c.215+15633C>G	NP_001269474.1:n.215+15633C>G
NM_001282548.1:c.158+27984C>G	NP_001269477.1:n.158+27984C>G
NM_001282549.1:c.364+10869C>G	NP_001269478.1:n.364+10869C>G
NR_104212.1:n.439C>G
NR_104215.1:n.382C>G
NR_104216.1:n.506+10869C>G
XM_011511567.1:c.392C>G	XP_011509869.1:p.Pro131Arg
XM_011511568.1:c.446C>G	XP_011509870.1:p.Pro149Arg
XM_017004613.1:c.545C>G	XP_016860102.1:p.Pro182Arg
XM_017004614.1:c.545C>G	XP_016860103.1:p.Pro182Arg
XR_002959322.1:n.636C>G
NM_000465.4:c.446C>G MANE Select	NP_000456.2:p.Pro149Arg
NM_001282543.2:c.389C>G	NP_001269472.1:p.Pro130Arg
NM_001282545.2:c.215+15633C>G	NP_001269474.1:n.215+15633C>G
NM_001282548.2:c.158+27984C>G	NP_001269477.1:n.158+27984C>G
NM_001282549.2:c.364+10869C>G	NP_001269478.1:n.364+10869C>G
NR_104212.2:n.411C>G
NR_104215.2:n.354C>G
NR_104216.2:n.478+10869C>G