Canonical Allele Identifier: CA350457794

Gene: BARD1

Linked Data

• MyVariant Identifiers: chr2:g.215646162A>T (hg19) ; chr2:g.214781438A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214781438A>T , CM000664.2:g.214781438A>T	GRCh38
NC_000002.11:g.215646162A>T , CM000664.1:g.215646162A>T	GRCh37
NC_000002.10:g.215354407A>T	NCBI36
NG_012047.2:g.33267T>A
NG_012047.3:g.33274T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.436T>A MANE Select	ENSP00000260947.4:p.Trp146Arg
ENST00000421162.2:c.215+15623T>A	ENSP00000392245.2:n.215+15623T>A
ENST00000613192.2:c.158+27974T>A	ENSP00000483275.2:n.158+27974T>A
ENST00000613374.5:c.158+27974T>A	ENSP00000484464.1:n.158+27974T>A
ENST00000613706.5:c.436T>A	ENSP00000484976.2:p.Trp146Arg
ENST00000617164.5:c.379T>A	ENSP00000480470.1:p.Trp127Arg
ENST00000619009.5:c.364+10859T>A	ENSP00000482293.1:n.364+10859T>A
ENST00000650978.1:c.278T>A
ENST00000260947.8:c.436T>A	ENSP00000260947.4:p.Trp146Arg
ENST00000421162.1:c.215+15623T>A	ENSP00000392245.1:n.215+15623T>A
ENST00000455743.5:c.*56T>A	ENSP00000412186.1:n.*56T>A
ENST00000471787.1:n.331T>A
ENST00000613192.1:c.73+27974T>A	ENSP00000483275.1:n.73+27974T>A
ENST00000613374.4:c.158+27974T>A	ENSP00000484464.1:n.158+27974T>A
ENST00000613706.4:c.215+15623T>A	ENSP00000484976.1:n.215+15623T>A
ENST00000617164.4:c.379T>A	ENSP00000480470.1:p.Trp127Arg
ENST00000619009.4:c.364+10859T>A	ENSP00000482293.1:n.364+10859T>A
ENST00000620057.4:c.364+10859T>A	ENSP00000481988.1:n.364+10859T>A
NM_000465.3:c.436T>A	NP_000456.2:p.Trp146Arg
NM_001282543.1:c.379T>A	NP_001269472.1:p.Trp127Arg
NM_001282545.1:c.215+15623T>A	NP_001269474.1:n.215+15623T>A
NM_001282548.1:c.158+27974T>A	NP_001269477.1:n.158+27974T>A
NM_001282549.1:c.364+10859T>A	NP_001269478.1:n.364+10859T>A
NR_104212.1:n.429T>A
NR_104215.1:n.372T>A
NR_104216.1:n.506+10859T>A
XM_011511567.1:c.382T>A	XP_011509869.1:p.Trp128Arg
XM_011511568.1:c.436T>A	XP_011509870.1:p.Trp146Arg
XM_017004613.1:c.535T>A	XP_016860102.1:p.Trp179Arg
XM_017004614.1:c.535T>A	XP_016860103.1:p.Trp179Arg
XR_002959322.1:n.626T>A
NM_000465.4:c.436T>A MANE Select	NP_000456.2:p.Trp146Arg
NM_001282543.2:c.379T>A	NP_001269472.1:p.Trp127Arg
NM_001282545.2:c.215+15623T>A	NP_001269474.1:n.215+15623T>A
NM_001282548.2:c.158+27974T>A	NP_001269477.1:n.158+27974T>A
NM_001282549.2:c.364+10859T>A	NP_001269478.1:n.364+10859T>A
NR_104212.2:n.401T>A
NR_104215.2:n.344T>A
NR_104216.2:n.478+10859T>A