Canonical Allele Identifier: CA350457457

Gene: BARD1

Linked Data

• MyVariant Identifiers: chr2:g.215646070C>A (hg19) ; chr2:g.214781346C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214781346C>A , CM000664.2:g.214781346C>A	GRCh38
NC_000002.11:g.215646070C>A , CM000664.1:g.215646070C>A	GRCh37
NC_000002.10:g.215354315C>A	NCBI36
NG_012047.2:g.33359G>T
NG_012047.3:g.33366G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.528G>T MANE Select	ENSP00000260947.4:p.Gln176His
ENST00000421162.2:c.215+15715G>T	ENSP00000392245.2:n.215+15715G>T
ENST00000613192.2:c.158+28066G>T	ENSP00000483275.2:n.158+28066G>T
ENST00000613374.5:c.158+28066G>T	ENSP00000484464.1:n.158+28066G>T
ENST00000613706.5:c.528G>T	ENSP00000484976.2:p.Gln176His
ENST00000617164.5:c.471G>T	ENSP00000480470.1:p.Gln157His
ENST00000619009.5:c.364+10951G>T	ENSP00000482293.1:n.364+10951G>T
ENST00000650978.1:c.370G>T
ENST00000260947.8:c.528G>T	ENSP00000260947.4:p.Gln176His
ENST00000421162.1:c.215+15715G>T	ENSP00000392245.1:n.215+15715G>T
ENST00000455743.5:c.*148G>T	ENSP00000412186.1:n.*148G>T
ENST00000471787.1:n.423G>T
ENST00000613192.1:c.73+28066G>T	ENSP00000483275.1:n.73+28066G>T
ENST00000613374.4:c.158+28066G>T	ENSP00000484464.1:n.158+28066G>T
ENST00000613706.4:c.215+15715G>T	ENSP00000484976.1:n.215+15715G>T
ENST00000617164.4:c.471G>T	ENSP00000480470.1:p.Gln157His
ENST00000619009.4:c.364+10951G>T	ENSP00000482293.1:n.364+10951G>T
ENST00000620057.4:c.364+10951G>T	ENSP00000481988.1:n.364+10951G>T
NM_000465.3:c.528G>T	NP_000456.2:p.Gln176His
NM_001282543.1:c.471G>T	NP_001269472.1:p.Gln157His
NM_001282545.1:c.215+15715G>T	NP_001269474.1:n.215+15715G>T
NM_001282548.1:c.158+28066G>T	NP_001269477.1:n.158+28066G>T
NM_001282549.1:c.364+10951G>T	NP_001269478.1:n.364+10951G>T
NR_104212.1:n.521G>T
NR_104215.1:n.464G>T
NR_104216.1:n.506+10951G>T
XM_011511567.1:c.474G>T	XP_011509869.1:p.Gln158His
XM_011511568.1:c.528G>T	XP_011509870.1:p.Gln176His
XM_017004613.1:c.627G>T	XP_016860102.1:p.Gln209His
XM_017004614.1:c.627G>T	XP_016860103.1:p.Gln209His
XR_002959322.1:n.718G>T
NM_000465.4:c.528G>T MANE Select	NP_000456.2:p.Gln176His
NM_001282543.2:c.471G>T	NP_001269472.1:p.Gln157His
NM_001282545.2:c.215+15715G>T	NP_001269474.1:n.215+15715G>T
NM_001282548.2:c.158+28066G>T	NP_001269477.1:n.158+28066G>T
NM_001282549.2:c.364+10951G>T	NP_001269478.1:n.364+10951G>T
NR_104212.2:n.493G>T
NR_104215.2:n.436G>T
NR_104216.2:n.478+10951G>T