Canonical Allele Identifier: CA1327046425

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214730507C= , CM000664.2:g.214730507C=	GRCh38
NC_000002.11:g.215595231C= , CM000664.1:g.215595231C=	GRCh37
NC_000002.10:g.215303476C=	NCBI36
NG_012047.2:g.84198G=
NG_012047.3:g.84205G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1905G= MANE Select	ENSP00000260947.4:p.Trp635=
ENST00000421162.2:c.552G=	ENSP00000392245.2:p.Trp184=
ENST00000613192.2:c.160G=	ENSP00000483275.2:p.Gly54=
ENST00000613374.5:c.495G=	ENSP00000484464.1:p.Trp165=
ENST00000613706.5:c.1497G=	ENSP00000484976.2:p.Trp499=
ENST00000617164.5:c.1848G=	ENSP00000480470.1:p.Trp616=
ENST00000619009.5:c.366G=	ENSP00000482293.1:p.Gly122=
ENST00000650978.1:c.3280G=
ENST00000260947.8:c.1905G=	ENSP00000260947.4:p.Trp635=
ENST00000421162.1:c.552G=	ENSP00000392245.1:p.Trp184=
ENST00000432456.5:c.2G=
ENST00000455743.5:c.*1525G=	ENSP00000412186.1:n.*1525G=
ENST00000471590.5:n.240G=
ENST00000613192.1:c.75G=	ENSP00000483275.1:p.Gly25=
ENST00000613374.4:c.495G=	ENSP00000484464.1:p.Trp165=
ENST00000613706.4:c.552G=	ENSP00000484976.1:p.Trp184=
ENST00000617164.4:c.1848G=	ENSP00000480470.1:p.Trp616=
ENST00000619009.4:c.366G=	ENSP00000482293.1:p.Gly122=
ENST00000620057.4:c.*571G=	ENSP00000481988.1:n.*571G=
NM_000465.3:c.1905G=	NP_000456.2:p.Trp635=
NM_001282543.1:c.1848G=	NP_001269472.1:p.Trp616=
NM_001282545.1:c.552G=	NP_001269474.1:p.Trp184=
NM_001282548.1:c.495G=	NP_001269477.1:p.Trp165=
NM_001282549.1:c.366G=	NP_001269478.1:p.Gly122=
NR_104212.1:n.1898G=
NR_104215.1:n.1841G=
NR_104216.1:n.1097G=
XM_011511567.1:c.1851G=	XP_011509869.1:p.Trp617=
XM_017004613.1:c.2004G=	XP_016860102.1:p.Trp668=
XR_002959322.1:n.2095G=
NM_000465.4:c.1905G= MANE Select	NP_000456.2:p.Trp635=
NM_001282543.2:c.1848G=	NP_001269472.1:p.Trp616=
NM_001282545.2:c.552G=	NP_001269474.1:p.Trp184=
NM_001282548.2:c.495G=	NP_001269477.1:p.Trp165=
NM_001282549.2:c.366G=	NP_001269478.1:p.Gly122=
NR_104212.2:n.1870G=
NR_104215.2:n.1813G=
NR_104216.2:n.1069G=