Canonical Allele Identifier: CA431390599

Gene: BARD1

Linked Data

• ClinVar Variation Id: 1775116
• ClinVar RCV Id: RCV002392600
• MyVariant Identifiers: chr2:g.215645554A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780830A>C , CM000664.2:g.214780830A>C	GRCh38
NC_000002.11:g.215645554A>C , CM000664.1:g.215645554A>C	GRCh37
NC_000002.10:g.215353799A>C	NCBI36
NG_012047.2:g.33875T>G
NG_012047.3:g.33882T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.1044T>G MANE Select	ENSP00000260947.4:p.Val348=
ENST00000421162.2:c.215+16231T>G	ENSP00000392245.2:n.215+16231T>G
ENST00000613192.2:c.158+28582T>G	ENSP00000483275.2:n.158+28582T>G
ENST00000613374.5:c.159-28275T>G	ENSP00000484464.1:n.159-28275T>G
ENST00000613706.5:c.906+138T>G	ENSP00000484976.2:n.906+138T>G
ENST00000617164.5:c.987T>G	ENSP00000480470.1:p.Val329=
ENST00000619009.5:c.364+11467T>G	ENSP00000482293.1:n.364+11467T>G
ENST00000650978.1:c.886T>G
ENST00000260947.8:c.1044T>G	ENSP00000260947.4:p.Val348=
ENST00000421162.1:c.215+16231T>G	ENSP00000392245.1:n.215+16231T>G
ENST00000455743.5:c.*664T>G	ENSP00000412186.1:n.*664T>G
ENST00000613192.1:c.73+28582T>G	ENSP00000483275.1:n.73+28582T>G
ENST00000613374.4:c.159-28275T>G	ENSP00000484464.1:n.159-28275T>G
ENST00000613706.4:c.215+16231T>G	ENSP00000484976.1:n.215+16231T>G
ENST00000617164.4:c.987T>G	ENSP00000480470.1:p.Val329=
ENST00000619009.4:c.364+11467T>G	ENSP00000482293.1:n.364+11467T>G
ENST00000620057.4:c.364+11467T>G	ENSP00000481988.1:n.364+11467T>G
NM_000465.3:c.1044T>G	NP_000456.2:p.Val348=
NM_001282543.1:c.987T>G	NP_001269472.1:p.Val329=
NM_001282545.1:c.215+16231T>G	NP_001269474.1:n.215+16231T>G
NM_001282548.1:c.159-28275T>G	NP_001269477.1:n.159-28275T>G
NM_001282549.1:c.364+11467T>G	NP_001269478.1:n.364+11467T>G
NR_104212.1:n.1037T>G
NR_104215.1:n.980T>G
NR_104216.1:n.506+11467T>G
XM_011511567.1:c.990T>G	XP_011509869.1:p.Val330=
XM_011511568.1:c.1044T>G	XP_011509870.1:p.Val348=
XM_017004613.1:c.1143T>G	XP_016860102.1:p.Val381=
XM_017004614.1:c.1143T>G	XP_016860103.1:p.Val381=
XR_002959322.1:n.1234T>G
NM_000465.4:c.1044T>G MANE Select	NP_000456.2:p.Val348=
NM_001282543.2:c.987T>G	NP_001269472.1:p.Val329=
NM_001282545.2:c.215+16231T>G	NP_001269474.1:n.215+16231T>G
NM_001282548.2:c.159-28275T>G	NP_001269477.1:n.159-28275T>G
NM_001282549.2:c.364+11467T>G	NP_001269478.1:n.364+11467T>G
NR_104212.2:n.1009T>G
NR_104215.2:n.952T>G
NR_104216.2:n.478+11467T>G