Canonical Allele Identifier: CA1327045486

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214728745G= , CM000664.2:g.214728745G=	GRCh38
NC_000002.11:g.215593469G= , CM000664.1:g.215593469G=	GRCh37
NC_000002.10:g.215301714G=	NCBI36
NG_012047.2:g.85960C=
NG_012047.3:g.85967C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.2265C= MANE Select	ENSP00000260947.4:p.Val755=
ENST00000421162.2:c.912C=	ENSP00000392245.2:p.Val304=
ENST00000613192.2:c.*328C=	ENSP00000483275.2:n.*328C=
ENST00000613374.5:c.855C=	ENSP00000484464.1:p.Val285=
ENST00000613706.5:c.1857C=	ENSP00000484976.2:p.Val619=
ENST00000617164.5:c.2208C=	ENSP00000480470.1:p.Val736=
ENST00000619009.5:c.726C=	ENSP00000482293.1:p.Val242=
ENST00000650978.1:c.3640C=
ENST00000260947.8:c.2265C=	ENSP00000260947.4:p.Val755=
ENST00000432456.5:c.408C=
ENST00000455743.5:c.*1885C=	ENSP00000412186.1:n.*1885C=
ENST00000471590.5:n.600C=
ENST00000613192.1:c.435C=	ENSP00000483275.1:p.Val145=
ENST00000613374.4:c.855C=	ENSP00000484464.1:p.Val285=
ENST00000613706.4:c.912C=	ENSP00000484976.1:p.Val304=
ENST00000617164.4:c.2208C=	ENSP00000480470.1:p.Val736=
ENST00000619009.4:c.726C=	ENSP00000482293.1:p.Val242=
ENST00000620057.4:c.*931C=	ENSP00000481988.1:n.*931C=
NM_000465.3:c.2265C=	NP_000456.2:p.Val755=
NM_001282543.1:c.2208C=	NP_001269472.1:p.Val736=
NM_001282545.1:c.912C=	NP_001269474.1:p.Val304=
NM_001282548.1:c.855C=	NP_001269477.1:p.Val285=
NM_001282549.1:c.726C=	NP_001269478.1:p.Val242=
NR_104212.1:n.2258C=
NR_104215.1:n.2201C=
NR_104216.1:n.1457C=
XM_011511567.1:c.2211C=	XP_011509869.1:p.Val737=
XM_017004613.1:c.2364C=	XP_016860102.1:p.Val788=
XR_002959322.1:n.2631C=
NM_000465.4:c.2265C= MANE Select	NP_000456.2:p.Val755=
NM_001282543.2:c.2208C=	NP_001269472.1:p.Val736=
NM_001282545.2:c.912C=	NP_001269474.1:p.Val304=
NM_001282548.2:c.855C=	NP_001269477.1:p.Val285=
NM_001282549.2:c.726C=	NP_001269478.1:p.Val242=
NR_104212.2:n.2230C=
NR_104215.2:n.2173C=
NR_104216.2:n.1429C=