Canonical Allele Identifier: CA350454003

Gene: BARD1

Linked Data

• ClinVar Variation Id: 951828
• ClinVar RCV Id: RCV001223823
• dbSNP Id: rs1694958957
• MyVariant Identifiers: chr2:g.215645469C>G (hg19) ; chr2:g.214780745C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780745C>G , CM000664.2:g.214780745C>G	GRCh38
NC_000002.11:g.215645469C>G , CM000664.1:g.215645469C>G	GRCh37
NC_000002.10:g.215353714C>G	NCBI36
NG_012047.2:g.33960G>C
NG_012047.3:g.33967G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1129G>C MANE Select	ENSP00000260947.4:p.Gly377Arg
ENST00000421162.2:c.215+16316G>C	ENSP00000392245.2:n.215+16316G>C
ENST00000613192.2:c.158+28667G>C	ENSP00000483275.2:n.158+28667G>C
ENST00000613374.5:c.159-28190G>C	ENSP00000484464.1:n.159-28190G>C
ENST00000613706.5:c.906+223G>C	ENSP00000484976.2:n.906+223G>C
ENST00000617164.5:c.1072G>C	ENSP00000480470.1:p.Gly358Arg
ENST00000619009.5:c.364+11552G>C	ENSP00000482293.1:n.364+11552G>C
ENST00000650978.1:c.971G>C
ENST00000260947.8:c.1129G>C	ENSP00000260947.4:p.Gly377Arg
ENST00000421162.1:c.215+16316G>C	ENSP00000392245.1:n.215+16316G>C
ENST00000455743.5:c.*749G>C	ENSP00000412186.1:n.*749G>C
ENST00000613192.1:c.73+28667G>C	ENSP00000483275.1:n.73+28667G>C
ENST00000613374.4:c.159-28190G>C	ENSP00000484464.1:n.159-28190G>C
ENST00000613706.4:c.215+16316G>C	ENSP00000484976.1:n.215+16316G>C
ENST00000617164.4:c.1072G>C	ENSP00000480470.1:p.Gly358Arg
ENST00000619009.4:c.364+11552G>C	ENSP00000482293.1:n.364+11552G>C
ENST00000620057.4:c.365-11433G>C	ENSP00000481988.1:n.365-11433G>C
NM_000465.3:c.1129G>C	NP_000456.2:p.Gly377Arg
NM_001282543.1:c.1072G>C	NP_001269472.1:p.Gly358Arg
NM_001282545.1:c.215+16316G>C	NP_001269474.1:n.215+16316G>C
NM_001282548.1:c.159-28190G>C	NP_001269477.1:n.159-28190G>C
NM_001282549.1:c.364+11552G>C	NP_001269478.1:n.364+11552G>C
NR_104212.1:n.1122G>C
NR_104215.1:n.1065G>C
NR_104216.1:n.507-11433G>C
XM_011511567.1:c.1075G>C	XP_011509869.1:p.Gly359Arg
XM_011511568.1:c.1129G>C	XP_011509870.1:p.Gly377Arg
XM_017004613.1:c.1228G>C	XP_016860102.1:p.Gly410Arg
XM_017004614.1:c.1228G>C	XP_016860103.1:p.Gly410Arg
XR_002959322.1:n.1319G>C
NM_000465.4:c.1129G>C MANE Select	NP_000456.2:p.Gly377Arg
NM_001282543.2:c.1072G>C	NP_001269472.1:p.Gly358Arg
NM_001282545.2:c.215+16316G>C	NP_001269474.1:n.215+16316G>C
NM_001282548.2:c.159-28190G>C	NP_001269477.1:n.159-28190G>C
NM_001282549.2:c.364+11552G>C	NP_001269478.1:n.364+11552G>C
NR_104212.2:n.1094G>C
NR_104215.2:n.1037G>C
NR_104216.2:n.479-11433G>C