Canonical Allele Identifier: CA1327045536

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214728803T= , CM000664.2:g.214728803T=	GRCh38
NC_000002.11:g.215593527T= , CM000664.1:g.215593527T=	GRCh37
NC_000002.10:g.215301772T=	NCBI36
NG_012047.2:g.85902A=
NG_012047.3:g.85909A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.2207A= MANE Select	ENSP00000260947.4:p.Tyr736=
ENST00000421162.2:c.854A=	ENSP00000392245.2:p.Tyr285=
ENST00000613192.2:c.*270A=	ENSP00000483275.2:n.*270A=
ENST00000613374.5:c.797A=	ENSP00000484464.1:p.Tyr266=
ENST00000613706.5:c.1799A=	ENSP00000484976.2:p.Tyr600=
ENST00000617164.5:c.2150A=	ENSP00000480470.1:p.Tyr717=
ENST00000619009.5:c.668A=	ENSP00000482293.1:p.Tyr223=
ENST00000650978.1:c.3582A=
ENST00000260947.8:c.2207A=	ENSP00000260947.4:p.Tyr736=
ENST00000432456.5:c.350A=
ENST00000455743.5:c.*1827A=	ENSP00000412186.1:n.*1827A=
ENST00000471590.5:n.542A=
ENST00000613192.1:c.377A=	ENSP00000483275.1:p.Tyr126=
ENST00000613374.4:c.797A=	ENSP00000484464.1:p.Tyr266=
ENST00000613706.4:c.854A=	ENSP00000484976.1:p.Tyr285=
ENST00000617164.4:c.2150A=	ENSP00000480470.1:p.Tyr717=
ENST00000619009.4:c.668A=	ENSP00000482293.1:p.Tyr223=
ENST00000620057.4:c.*873A=	ENSP00000481988.1:n.*873A=
NM_000465.3:c.2207A=	NP_000456.2:p.Tyr736=
NM_001282543.1:c.2150A=	NP_001269472.1:p.Tyr717=
NM_001282545.1:c.854A=	NP_001269474.1:p.Tyr285=
NM_001282548.1:c.797A=	NP_001269477.1:p.Tyr266=
NM_001282549.1:c.668A=	NP_001269478.1:p.Tyr223=
NR_104212.1:n.2200A=
NR_104215.1:n.2143A=
NR_104216.1:n.1399A=
XM_011511567.1:c.2153A=	XP_011509869.1:p.Tyr718=
XM_017004613.1:c.2306A=	XP_016860102.1:p.Tyr769=
XR_002959322.1:n.2573A=
NM_000465.4:c.2207A= MANE Select	NP_000456.2:p.Tyr736=
NM_001282543.2:c.2150A=	NP_001269472.1:p.Tyr717=
NM_001282545.2:c.854A=	NP_001269474.1:p.Tyr285=
NM_001282548.2:c.797A=	NP_001269477.1:p.Tyr266=
NM_001282549.2:c.668A=	NP_001269478.1:p.Tyr223=
NR_104212.2:n.2172A=
NR_104215.2:n.2115A=
NR_104216.2:n.1371A=