Canonical Allele Identifier: CA1327053324

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214745085A= , CM000664.2:g.214745085A=	GRCh38
NC_000002.11:g.215609809A= , CM000664.1:g.215609809A=	GRCh37
NC_000002.10:g.215318054A=	NCBI36
NG_012047.2:g.69620T=
NG_012047.3:g.69627T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1885T= MANE Select	ENSP00000260947.4:p.Trp629=
ENST00000421162.2:c.532T=	ENSP00000392245.2:p.Trp178=
ENST00000613192.2:c.159-14577T=	ENSP00000483275.2:n.159-14577T=
ENST00000613374.5:c.475T=	ENSP00000484464.1:p.Trp159=
ENST00000613706.5:c.1477T=	ENSP00000484976.2:p.Trp493=
ENST00000617164.5:c.1828T=	ENSP00000480470.1:p.Trp610=
ENST00000619009.5:c.365-14577T=	ENSP00000482293.1:n.365-14577T=
ENST00000650978.1:c.3260T=
ENST00000260947.8:c.1885T=	ENSP00000260947.4:p.Trp629=
ENST00000421162.1:c.532T=	ENSP00000392245.1:p.Trp178=
ENST00000455743.5:c.*1505T=	ENSP00000412186.1:n.*1505T=
ENST00000613192.1:c.74-14577T=	ENSP00000483275.1:n.74-14577T=
ENST00000613374.4:c.475T=	ENSP00000484464.1:p.Trp159=
ENST00000613706.4:c.532T=	ENSP00000484976.1:p.Trp178=
ENST00000617164.4:c.1828T=	ENSP00000480470.1:p.Trp610=
ENST00000619009.4:c.365-14577T=	ENSP00000482293.1:n.365-14577T=
ENST00000620057.4:c.*551T=	ENSP00000481988.1:n.*551T=
NM_000465.3:c.1885T=	NP_000456.2:p.Trp629=
NM_001282543.1:c.1828T=	NP_001269472.1:p.Trp610=
NM_001282545.1:c.532T=	NP_001269474.1:p.Trp178=
NM_001282548.1:c.475T=	NP_001269477.1:p.Trp159=
NM_001282549.1:c.365-14577T=	NP_001269478.1:n.365-14577T=
NR_104212.1:n.1878T=
NR_104215.1:n.1821T=
NR_104216.1:n.1077T=
XM_011511567.1:c.1831T=	XP_011509869.1:p.Trp611=
XM_011511568.1:c.1885T=	XP_011509870.1:p.Trp629=
XM_017004613.1:c.1984T=	XP_016860102.1:p.Trp662=
XM_017004614.1:c.1984T=	XP_016860103.1:p.Trp662=
XR_002959322.1:n.2075T=
NM_000465.4:c.1885T= MANE Select	NP_000456.2:p.Trp629=
NM_001282543.2:c.1828T=	NP_001269472.1:p.Trp610=
NM_001282545.2:c.532T=	NP_001269474.1:p.Trp178=
NM_001282548.2:c.475T=	NP_001269477.1:p.Trp159=
NM_001282549.2:c.365-14577T=	NP_001269478.1:n.365-14577T=
NR_104212.2:n.1850T=
NR_104215.2:n.1793T=
NR_104216.2:n.1049T=