Canonical Allele Identifier: CA350451109

Gene: BARD1

Linked Data

• MyVariant Identifiers: chr2:g.215595149T>C (hg19) ; chr2:g.214730425T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214730425T>C , CM000664.2:g.214730425T>C	GRCh38
NC_000002.11:g.215595149T>C , CM000664.1:g.215595149T>C	GRCh37
NC_000002.10:g.215303394T>C	NCBI36
NG_012047.2:g.84280A>G
NG_012047.3:g.84287A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1987A>G MANE Select	ENSP00000260947.4:p.Asn663Asp
ENST00000421162.2:c.634A>G	ENSP00000392245.2:p.Asn212Asp
ENST00000613192.2:c.*50A>G	ENSP00000483275.2:n.*50A>G
ENST00000613374.5:c.577A>G	ENSP00000484464.1:p.Asn193Asp
ENST00000613706.5:c.1579A>G	ENSP00000484976.2:p.Asn527Asp
ENST00000617164.5:c.1930A>G	ENSP00000480470.1:p.Asn644Asp
ENST00000619009.5:c.448A>G	ENSP00000482293.1:p.Asn150Asp
ENST00000650978.1:c.3362A>G
ENST00000260947.8:c.1987A>G	ENSP00000260947.4:p.Asn663Asp
ENST00000421162.1:c.634A>G	ENSP00000392245.1:p.Asn212Asp
ENST00000432456.5:c.84A>G
ENST00000455743.5:c.*1607A>G	ENSP00000412186.1:n.*1607A>G
ENST00000471590.5:n.322A>G
ENST00000613192.1:c.157A>G	ENSP00000483275.1:p.Asn53Asp
ENST00000613374.4:c.577A>G	ENSP00000484464.1:p.Asn193Asp
ENST00000613706.4:c.634A>G	ENSP00000484976.1:p.Asn212Asp
ENST00000617164.4:c.1930A>G	ENSP00000480470.1:p.Asn644Asp
ENST00000619009.4:c.448A>G	ENSP00000482293.1:p.Asn150Asp
ENST00000620057.4:c.*653A>G	ENSP00000481988.1:n.*653A>G
NM_000465.3:c.1987A>G	NP_000456.2:p.Asn663Asp
NM_001282543.1:c.1930A>G	NP_001269472.1:p.Asn644Asp
NM_001282545.1:c.634A>G	NP_001269474.1:p.Asn212Asp
NM_001282548.1:c.577A>G	NP_001269477.1:p.Asn193Asp
NM_001282549.1:c.448A>G	NP_001269478.1:p.Asn150Asp
NR_104212.1:n.1980A>G
NR_104215.1:n.1923A>G
NR_104216.1:n.1179A>G
XM_011511567.1:c.1933A>G	XP_011509869.1:p.Asn645Asp
XM_017004613.1:c.2086A>G	XP_016860102.1:p.Asn696Asp
XR_002959322.1:n.2177A>G
NM_000465.4:c.1987A>G MANE Select	NP_000456.2:p.Asn663Asp
NM_001282543.2:c.1930A>G	NP_001269472.1:p.Asn644Asp
NM_001282545.2:c.634A>G	NP_001269474.1:p.Asn212Asp
NM_001282548.2:c.577A>G	NP_001269477.1:p.Asn193Asp
NM_001282549.2:c.448A>G	NP_001269478.1:p.Asn150Asp
NR_104212.2:n.1952A>G
NR_104215.2:n.1895A>G
NR_104216.2:n.1151A>G