Canonical Allele Identifier: CA1327053322

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214745083C= , CM000664.2:g.214745083C=	GRCh38
NC_000002.11:g.215609807C= , CM000664.1:g.215609807C=	GRCh37
NC_000002.10:g.215318052C=	NCBI36
NG_012047.2:g.69622G=
NG_012047.3:g.69629G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1887G= MANE Select	ENSP00000260947.4:p.Trp629=
ENST00000421162.2:c.534G=	ENSP00000392245.2:p.Trp178=
ENST00000613192.2:c.159-14575G=	ENSP00000483275.2:n.159-14575G=
ENST00000613374.5:c.477G=	ENSP00000484464.1:p.Trp159=
ENST00000613706.5:c.1479G=	ENSP00000484976.2:p.Trp493=
ENST00000617164.5:c.1830G=	ENSP00000480470.1:p.Trp610=
ENST00000619009.5:c.365-14575G=	ENSP00000482293.1:n.365-14575G=
ENST00000650978.1:c.3262G=
ENST00000260947.8:c.1887G=	ENSP00000260947.4:p.Trp629=
ENST00000421162.1:c.534G=	ENSP00000392245.1:p.Trp178=
ENST00000455743.5:c.*1507G=	ENSP00000412186.1:n.*1507G=
ENST00000613192.1:c.74-14575G=	ENSP00000483275.1:n.74-14575G=
ENST00000613374.4:c.477G=	ENSP00000484464.1:p.Trp159=
ENST00000613706.4:c.534G=	ENSP00000484976.1:p.Trp178=
ENST00000617164.4:c.1830G=	ENSP00000480470.1:p.Trp610=
ENST00000619009.4:c.365-14575G=	ENSP00000482293.1:n.365-14575G=
ENST00000620057.4:c.*553G=	ENSP00000481988.1:n.*553G=
NM_000465.3:c.1887G=	NP_000456.2:p.Trp629=
NM_001282543.1:c.1830G=	NP_001269472.1:p.Trp610=
NM_001282545.1:c.534G=	NP_001269474.1:p.Trp178=
NM_001282548.1:c.477G=	NP_001269477.1:p.Trp159=
NM_001282549.1:c.365-14575G=	NP_001269478.1:n.365-14575G=
NR_104212.1:n.1880G=
NR_104215.1:n.1823G=
NR_104216.1:n.1079G=
XM_011511567.1:c.1833G=	XP_011509869.1:p.Trp611=
XM_011511568.1:c.1887G=	XP_011509870.1:p.Trp629=
XM_017004613.1:c.1986G=	XP_016860102.1:p.Trp662=
XM_017004614.1:c.1986G=	XP_016860103.1:p.Trp662=
XR_002959322.1:n.2077G=
NM_000465.4:c.1887G= MANE Select	NP_000456.2:p.Trp629=
NM_001282543.2:c.1830G=	NP_001269472.1:p.Trp610=
NM_001282545.2:c.534G=	NP_001269474.1:p.Trp178=
NM_001282548.2:c.477G=	NP_001269477.1:p.Trp159=
NM_001282549.2:c.365-14575G=	NP_001269478.1:n.365-14575G=
NR_104212.2:n.1852G=
NR_104215.2:n.1795G=
NR_104216.2:n.1051G=