Canonical Allele Identifier: CA350451155

Gene: BARD1

Linked Data

• MyVariant Identifiers: chr2:g.215595175G>T (hg19) ; chr2:g.214730451G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214730451G>T , CM000664.2:g.214730451G>T	GRCh38
NC_000002.11:g.215595175G>T , CM000664.1:g.215595175G>T	GRCh37
NC_000002.10:g.215303420G>T	NCBI36
NG_012047.2:g.84254C>A
NG_012047.3:g.84261C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1961C>A MANE Select	ENSP00000260947.4:p.Pro654His
ENST00000421162.2:c.608C>A	ENSP00000392245.2:p.Pro203His
ENST00000613192.2:c.*24C>A	ENSP00000483275.2:n.*24C>A
ENST00000613374.5:c.551C>A	ENSP00000484464.1:p.Pro184His
ENST00000613706.5:c.1553C>A	ENSP00000484976.2:p.Pro518His
ENST00000617164.5:c.1904C>A	ENSP00000480470.1:p.Pro635His
ENST00000619009.5:c.422C>A	ENSP00000482293.1:p.Pro141His
ENST00000650978.1:c.3336C>A
ENST00000260947.8:c.1961C>A	ENSP00000260947.4:p.Pro654His
ENST00000421162.1:c.608C>A	ENSP00000392245.1:p.Pro203His
ENST00000432456.5:c.58C>A
ENST00000455743.5:c.*1581C>A	ENSP00000412186.1:n.*1581C>A
ENST00000471590.5:n.296C>A
ENST00000613192.1:c.131C>A	ENSP00000483275.1:p.Pro44His
ENST00000613374.4:c.551C>A	ENSP00000484464.1:p.Pro184His
ENST00000613706.4:c.608C>A	ENSP00000484976.1:p.Pro203His
ENST00000617164.4:c.1904C>A	ENSP00000480470.1:p.Pro635His
ENST00000619009.4:c.422C>A	ENSP00000482293.1:p.Pro141His
ENST00000620057.4:c.*627C>A	ENSP00000481988.1:n.*627C>A
NM_000465.3:c.1961C>A	NP_000456.2:p.Pro654His
NM_001282543.1:c.1904C>A	NP_001269472.1:p.Pro635His
NM_001282545.1:c.608C>A	NP_001269474.1:p.Pro203His
NM_001282548.1:c.551C>A	NP_001269477.1:p.Pro184His
NM_001282549.1:c.422C>A	NP_001269478.1:p.Pro141His
NR_104212.1:n.1954C>A
NR_104215.1:n.1897C>A
NR_104216.1:n.1153C>A
XM_011511567.1:c.1907C>A	XP_011509869.1:p.Pro636His
XM_017004613.1:c.2060C>A	XP_016860102.1:p.Pro687His
XR_002959322.1:n.2151C>A
NM_000465.4:c.1961C>A MANE Select	NP_000456.2:p.Pro654His
NM_001282543.2:c.1904C>A	NP_001269472.1:p.Pro635His
NM_001282545.2:c.608C>A	NP_001269474.1:p.Pro203His
NM_001282548.2:c.551C>A	NP_001269477.1:p.Pro184His
NM_001282549.2:c.422C>A	NP_001269478.1:p.Pro141His
NR_104212.2:n.1926C>A
NR_104215.2:n.1869C>A
NR_104216.2:n.1125C>A