Canonical Allele Identifier: CA350457434

Gene: BARD1

Linked Data

• MyVariant Identifiers: chr2:g.215646060A>T (hg19) ; chr2:g.214781336A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214781336A>T , CM000664.2:g.214781336A>T	GRCh38
NC_000002.11:g.215646060A>T , CM000664.1:g.215646060A>T	GRCh37
NC_000002.10:g.215354305A>T	NCBI36
NG_012047.2:g.33369T>A
NG_012047.3:g.33376T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.538T>A MANE Select	ENSP00000260947.4:p.Tyr180Asn
ENST00000421162.2:c.215+15725T>A	ENSP00000392245.2:n.215+15725T>A
ENST00000613192.2:c.158+28076T>A	ENSP00000483275.2:n.158+28076T>A
ENST00000613374.5:c.158+28076T>A	ENSP00000484464.1:n.158+28076T>A
ENST00000613706.5:c.538T>A	ENSP00000484976.2:p.Tyr180Asn
ENST00000617164.5:c.481T>A	ENSP00000480470.1:p.Tyr161Asn
ENST00000619009.5:c.364+10961T>A	ENSP00000482293.1:n.364+10961T>A
ENST00000650978.1:c.380T>A
ENST00000260947.8:c.538T>A	ENSP00000260947.4:p.Tyr180Asn
ENST00000421162.1:c.215+15725T>A	ENSP00000392245.1:n.215+15725T>A
ENST00000455743.5:c.*158T>A	ENSP00000412186.1:n.*158T>A
ENST00000471787.1:n.433T>A
ENST00000613192.1:c.73+28076T>A	ENSP00000483275.1:n.73+28076T>A
ENST00000613374.4:c.158+28076T>A	ENSP00000484464.1:n.158+28076T>A
ENST00000613706.4:c.215+15725T>A	ENSP00000484976.1:n.215+15725T>A
ENST00000617164.4:c.481T>A	ENSP00000480470.1:p.Tyr161Asn
ENST00000619009.4:c.364+10961T>A	ENSP00000482293.1:n.364+10961T>A
ENST00000620057.4:c.364+10961T>A	ENSP00000481988.1:n.364+10961T>A
NM_000465.3:c.538T>A	NP_000456.2:p.Tyr180Asn
NM_001282543.1:c.481T>A	NP_001269472.1:p.Tyr161Asn
NM_001282545.1:c.215+15725T>A	NP_001269474.1:n.215+15725T>A
NM_001282548.1:c.158+28076T>A	NP_001269477.1:n.158+28076T>A
NM_001282549.1:c.364+10961T>A	NP_001269478.1:n.364+10961T>A
NR_104212.1:n.531T>A
NR_104215.1:n.474T>A
NR_104216.1:n.506+10961T>A
XM_011511567.1:c.484T>A	XP_011509869.1:p.Tyr162Asn
XM_011511568.1:c.538T>A	XP_011509870.1:p.Tyr180Asn
XM_017004613.1:c.637T>A	XP_016860102.1:p.Tyr213Asn
XM_017004614.1:c.637T>A	XP_016860103.1:p.Tyr213Asn
XR_002959322.1:n.728T>A
NM_000465.4:c.538T>A MANE Select	NP_000456.2:p.Tyr180Asn
NM_001282543.2:c.481T>A	NP_001269472.1:p.Tyr161Asn
NM_001282545.2:c.215+15725T>A	NP_001269474.1:n.215+15725T>A
NM_001282548.2:c.158+28076T>A	NP_001269477.1:n.158+28076T>A
NM_001282549.2:c.364+10961T>A	NP_001269478.1:n.364+10961T>A
NR_104212.2:n.503T>A
NR_104215.2:n.446T>A
NR_104216.2:n.478+10961T>A