Canonical Allele Identifier: CA350453932

Gene: BARD1

Linked Data

• MyVariant Identifiers: chr2:g.215645440T>G (hg19) ; chr2:g.214780716T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214780716T>G , CM000664.2:g.214780716T>G	GRCh38
NC_000002.11:g.215645440T>G , CM000664.1:g.215645440T>G	GRCh37
NC_000002.10:g.215353685T>G	NCBI36
NG_012047.2:g.33989A>C
NG_012047.3:g.33996A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1158A>C MANE Select	ENSP00000260947.4:p.Glu386Asp
ENST00000421162.2:c.215+16345A>C	ENSP00000392245.2:n.215+16345A>C
ENST00000613192.2:c.158+28696A>C	ENSP00000483275.2:n.158+28696A>C
ENST00000613374.5:c.159-28161A>C	ENSP00000484464.1:n.159-28161A>C
ENST00000613706.5:c.906+252A>C	ENSP00000484976.2:n.906+252A>C
ENST00000617164.5:c.1101A>C	ENSP00000480470.1:p.Glu367Asp
ENST00000619009.5:c.364+11581A>C	ENSP00000482293.1:n.364+11581A>C
ENST00000650978.1:c.1000A>C
ENST00000260947.8:c.1158A>C	ENSP00000260947.4:p.Glu386Asp
ENST00000421162.1:c.215+16345A>C	ENSP00000392245.1:n.215+16345A>C
ENST00000455743.5:c.*778A>C	ENSP00000412186.1:n.*778A>C
ENST00000613192.1:c.73+28696A>C	ENSP00000483275.1:n.73+28696A>C
ENST00000613374.4:c.159-28161A>C	ENSP00000484464.1:n.159-28161A>C
ENST00000613706.4:c.215+16345A>C	ENSP00000484976.1:n.215+16345A>C
ENST00000617164.4:c.1101A>C	ENSP00000480470.1:p.Glu367Asp
ENST00000619009.4:c.364+11581A>C	ENSP00000482293.1:n.364+11581A>C
ENST00000620057.4:c.365-11404A>C	ENSP00000481988.1:n.365-11404A>C
NM_000465.3:c.1158A>C	NP_000456.2:p.Glu386Asp
NM_001282543.1:c.1101A>C	NP_001269472.1:p.Glu367Asp
NM_001282545.1:c.215+16345A>C	NP_001269474.1:n.215+16345A>C
NM_001282548.1:c.159-28161A>C	NP_001269477.1:n.159-28161A>C
NM_001282549.1:c.364+11581A>C	NP_001269478.1:n.364+11581A>C
NR_104212.1:n.1151A>C
NR_104215.1:n.1094A>C
NR_104216.1:n.507-11404A>C
XM_011511567.1:c.1104A>C	XP_011509869.1:p.Glu368Asp
XM_011511568.1:c.1158A>C	XP_011509870.1:p.Glu386Asp
XM_017004613.1:c.1257A>C	XP_016860102.1:p.Glu419Asp
XM_017004614.1:c.1257A>C	XP_016860103.1:p.Glu419Asp
XR_002959322.1:n.1348A>C
NM_000465.4:c.1158A>C MANE Select	NP_000456.2:p.Glu386Asp
NM_001282543.2:c.1101A>C	NP_001269472.1:p.Glu367Asp
NM_001282545.2:c.215+16345A>C	NP_001269474.1:n.215+16345A>C
NM_001282548.2:c.159-28161A>C	NP_001269477.1:n.159-28161A>C
NM_001282549.2:c.364+11581A>C	NP_001269478.1:n.364+11581A>C
NR_104212.2:n.1123A>C
NR_104215.2:n.1066A>C
NR_104216.2:n.479-11404A>C