Canonical Allele Identifier: CA1327046403

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214730477A= , CM000664.2:g.214730477A=	GRCh38
NC_000002.11:g.215595201A= , CM000664.1:g.215595201A=	GRCh37
NC_000002.10:g.215303446A=	NCBI36
NG_012047.2:g.84228T=
NG_012047.3:g.84235T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.1935T= MANE Select	ENSP00000260947.4:p.Cys645=
ENST00000421162.2:c.582T=	ENSP00000392245.2:p.Cys194=
ENST00000613192.2:c.190T=	ENSP00000483275.2:p.Ter64=
ENST00000613374.5:c.525T=	ENSP00000484464.1:p.Cys175=
ENST00000613706.5:c.1527T=	ENSP00000484976.2:p.Cys509=
ENST00000617164.5:c.1878T=	ENSP00000480470.1:p.Cys626=
ENST00000619009.5:c.396T=	ENSP00000482293.1:p.Cys132=
ENST00000650978.1:c.3310T=
ENST00000260947.8:c.1935T=	ENSP00000260947.4:p.Cys645=
ENST00000421162.1:c.582T=	ENSP00000392245.1:p.Cys194=
ENST00000432456.5:c.32T=
ENST00000455743.5:c.*1555T=	ENSP00000412186.1:n.*1555T=
ENST00000471590.5:n.270T=
ENST00000613192.1:c.105T=	ENSP00000483275.1:p.Cys35=
ENST00000613374.4:c.525T=	ENSP00000484464.1:p.Cys175=
ENST00000613706.4:c.582T=	ENSP00000484976.1:p.Cys194=
ENST00000617164.4:c.1878T=	ENSP00000480470.1:p.Cys626=
ENST00000619009.4:c.396T=	ENSP00000482293.1:p.Cys132=
ENST00000620057.4:c.*601T=	ENSP00000481988.1:n.*601T=
NM_000465.3:c.1935T=	NP_000456.2:p.Cys645=
NM_001282543.1:c.1878T=	NP_001269472.1:p.Cys626=
NM_001282545.1:c.582T=	NP_001269474.1:p.Cys194=
NM_001282548.1:c.525T=	NP_001269477.1:p.Cys175=
NM_001282549.1:c.396T=	NP_001269478.1:p.Cys132=
NR_104212.1:n.1928T=
NR_104215.1:n.1871T=
NR_104216.1:n.1127T=
XM_011511567.1:c.1881T=	XP_011509869.1:p.Cys627=
XM_017004613.1:c.2034T=	XP_016860102.1:p.Cys678=
XR_002959322.1:n.2125T=
NM_000465.4:c.1935T= MANE Select	NP_000456.2:p.Cys645=
NM_001282543.2:c.1878T=	NP_001269472.1:p.Cys626=
NM_001282545.2:c.582T=	NP_001269474.1:p.Cys194=
NM_001282548.2:c.525T=	NP_001269477.1:p.Cys175=
NM_001282549.2:c.396T=	NP_001269478.1:p.Cys132=
NR_104212.2:n.1900T=
NR_104215.2:n.1843T=
NR_104216.2:n.1099T=