Canonical Allele Identifier: CA431145988

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214745840C>T , CM000664.2:g.214745840C>T	GRCh38
NC_000002.11:g.215610564C>T , CM000664.1:g.215610564C>T	GRCh37
NC_000002.10:g.215318809C>T	NCBI36
NG_012047.2:g.68865G>A
NG_012047.3:g.68872G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000465.4:c.1692G>A MANE Select	NP_000456.2:p.Gln564=
ENST00000260947.9:c.1692G>A MANE Select	ENSP00000260947.4:p.Gln564=
NM_000465.3:c.1692G>A	NP_000456.2:p.Gln564=
NM_001282543.1:c.1635G>A	NP_001269472.1:p.Gln545=
NM_001282543.2:c.1635G>A	NP_001269472.1:p.Gln545=
NM_001282545.1:c.339G>A	NP_001269474.1:p.Gln113=
NM_001282545.2:c.339G>A	NP_001269474.1:p.Gln113=
NM_001282548.1:c.282G>A	NP_001269477.1:p.Gln94=
NM_001282548.2:c.282G>A	NP_001269477.1:p.Gln94=
NM_001282549.1:c.365-15332G>A	NP_001269478.1:n.365-15332G>A
NM_001282549.2:c.365-15332G>A	NP_001269478.1:n.365-15332G>A
NR_104212.1:n.1685G>A
NR_104212.2:n.1657G>A
NR_104215.1:n.1628G>A
NR_104215.2:n.1600G>A
NR_104216.1:n.884G>A
NR_104216.2:n.856G>A
ENST00000260947.8:c.1692G>A	ENSP00000260947.4:p.Gln564=
ENST00000421162.1:c.339G>A	ENSP00000392245.1:p.Gln113=
ENST00000421162.2:c.339G>A	ENSP00000392245.2:p.Gln113=
ENST00000455743.5:c.*1312G>A	ENSP00000412186.1:n.*1312G>A
ENST00000465841.1:n.47G>A
ENST00000613192.1:c.74-15332G>A	ENSP00000483275.1:n.74-15332G>A
ENST00000613192.2:c.159-15332G>A	ENSP00000483275.2:n.159-15332G>A
ENST00000613374.4:c.282G>A	ENSP00000484464.1:p.Gln94=
ENST00000613374.5:c.282G>A	ENSP00000484464.1:p.Gln94=
ENST00000613706.4:c.339G>A	ENSP00000484976.1:p.Gln113=
ENST00000613706.5:c.1284G>A	ENSP00000484976.2:p.Gln428=
ENST00000617164.4:c.1635G>A	ENSP00000480470.1:p.Gln545=
ENST00000617164.5:c.1635G>A	ENSP00000480470.1:p.Gln545=
ENST00000619009.4:c.365-15332G>A	ENSP00000482293.1:n.365-15332G>A
ENST00000619009.5:c.365-15332G>A	ENSP00000482293.1:n.365-15332G>A
ENST00000620057.4:c.*358G>A	ENSP00000481988.1:n.*358G>A
ENST00000650978.1:c.3067G>A
XM_011511567.1:c.1638G>A	XP_011509869.1:p.Gln546=
XM_011511568.1:c.1692G>A	XP_011509870.1:p.Gln564=
XM_017004613.1:c.1791G>A	XP_016860102.1:p.Gln597=
XM_017004614.1:c.1791G>A	XP_016860103.1:p.Gln597=
XR_002959322.1:n.1882G>A