Canonical Allele Identifier: CA350454037

Gene: BARD1

Linked Data

• ClinVar Variation Id: 1795248
• ClinVar RCV Id: RCV002431340
• MyVariant Identifiers: chr2:g.215645487T>C (hg19) ; chr2:g.214780763T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780763T>C , CM000664.2:g.214780763T>C	GRCh38
NC_000002.11:g.215645487T>C , CM000664.1:g.215645487T>C	GRCh37
NC_000002.10:g.215353732T>C	NCBI36
NG_012047.2:g.33942A>G
NG_012047.3:g.33949A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1111A>G MANE Select	ENSP00000260947.4:p.Lys371Glu
ENST00000421162.2:c.215+16298A>G	ENSP00000392245.2:n.215+16298A>G
ENST00000613192.2:c.158+28649A>G	ENSP00000483275.2:n.158+28649A>G
ENST00000613374.5:c.159-28208A>G	ENSP00000484464.1:n.159-28208A>G
ENST00000613706.5:c.906+205A>G	ENSP00000484976.2:n.906+205A>G
ENST00000617164.5:c.1054A>G	ENSP00000480470.1:p.Lys352Glu
ENST00000619009.5:c.364+11534A>G	ENSP00000482293.1:n.364+11534A>G
ENST00000650978.1:c.953A>G
ENST00000260947.8:c.1111A>G	ENSP00000260947.4:p.Lys371Glu
ENST00000421162.1:c.215+16298A>G	ENSP00000392245.1:n.215+16298A>G
ENST00000455743.5:c.*731A>G	ENSP00000412186.1:n.*731A>G
ENST00000613192.1:c.73+28649A>G	ENSP00000483275.1:n.73+28649A>G
ENST00000613374.4:c.159-28208A>G	ENSP00000484464.1:n.159-28208A>G
ENST00000613706.4:c.215+16298A>G	ENSP00000484976.1:n.215+16298A>G
ENST00000617164.4:c.1054A>G	ENSP00000480470.1:p.Lys352Glu
ENST00000619009.4:c.364+11534A>G	ENSP00000482293.1:n.364+11534A>G
ENST00000620057.4:c.365-11451A>G	ENSP00000481988.1:n.365-11451A>G
NM_000465.3:c.1111A>G	NP_000456.2:p.Lys371Glu
NM_001282543.1:c.1054A>G	NP_001269472.1:p.Lys352Glu
NM_001282545.1:c.215+16298A>G	NP_001269474.1:n.215+16298A>G
NM_001282548.1:c.159-28208A>G	NP_001269477.1:n.159-28208A>G
NM_001282549.1:c.364+11534A>G	NP_001269478.1:n.364+11534A>G
NR_104212.1:n.1104A>G
NR_104215.1:n.1047A>G
NR_104216.1:n.507-11451A>G
XM_011511567.1:c.1057A>G	XP_011509869.1:p.Lys353Glu
XM_011511568.1:c.1111A>G	XP_011509870.1:p.Lys371Glu
XM_017004613.1:c.1210A>G	XP_016860102.1:p.Lys404Glu
XM_017004614.1:c.1210A>G	XP_016860103.1:p.Lys404Glu
XR_002959322.1:n.1301A>G
NM_000465.4:c.1111A>G MANE Select	NP_000456.2:p.Lys371Glu
NM_001282543.2:c.1054A>G	NP_001269472.1:p.Lys352Glu
NM_001282545.2:c.215+16298A>G	NP_001269474.1:n.215+16298A>G
NM_001282548.2:c.159-28208A>G	NP_001269477.1:n.159-28208A>G
NM_001282549.2:c.364+11534A>G	NP_001269478.1:n.364+11534A>G
NR_104212.2:n.1076A>G
NR_104215.2:n.1019A>G
NR_104216.2:n.479-11451A>G