Canonical Allele Identifier: CA1327045433

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214728681T= , CM000664.2:g.214728681T=	GRCh38
NC_000002.11:g.215593405T= , CM000664.1:g.215593405T=	GRCh37
NC_000002.10:g.215301650T=	NCBI36
NG_012047.2:g.86024A=
NG_012047.3:g.86031A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.2329A= MANE Select	ENSP00000260947.4:p.Ser777=
ENST00000421162.2:c.976A=	ENSP00000392245.2:p.Ser326=
ENST00000613192.2:c.*392A=	ENSP00000483275.2:n.*392A=
ENST00000613374.5:c.919A=	ENSP00000484464.1:p.Ser307=
ENST00000613706.5:c.1921A=	ENSP00000484976.2:p.Ser641=
ENST00000617164.5:c.2272A=	ENSP00000480470.1:p.Ser758=
ENST00000619009.5:c.790A=	ENSP00000482293.1:p.Ser264=
ENST00000650978.1:c.3704A=
ENST00000260947.8:c.2329A=	ENSP00000260947.4:p.Ser777=
ENST00000432456.5:c.472A=
ENST00000471590.5:n.664A=
ENST00000613192.1:c.499A=	ENSP00000483275.1:p.Ser167=
ENST00000613374.4:c.919A=	ENSP00000484464.1:p.Ser307=
ENST00000613706.4:c.976A=	ENSP00000484976.1:p.Ser326=
ENST00000617164.4:c.2272A=	ENSP00000480470.1:p.Ser758=
ENST00000619009.4:c.790A=	ENSP00000482293.1:p.Ser264=
ENST00000620057.4:c.*995A=	ENSP00000481988.1:n.*995A=
NM_000465.3:c.2329A=	NP_000456.2:p.Ser777=
NM_001282543.1:c.2272A=	NP_001269472.1:p.Ser758=
NM_001282545.1:c.976A=	NP_001269474.1:p.Ser326=
NM_001282548.1:c.919A=	NP_001269477.1:p.Ser307=
NM_001282549.1:c.790A=	NP_001269478.1:p.Ser264=
NR_104212.1:n.2322A=
NR_104215.1:n.2265A=
NR_104216.1:n.1521A=
XM_011511567.1:c.2275A=	XP_011509869.1:p.Ser759=
XM_017004613.1:c.2428A=	XP_016860102.1:p.Ser810=
XR_002959322.1:n.2695A=
NM_000465.4:c.2329A= MANE Select	NP_000456.2:p.Ser777=
NM_001282543.2:c.2272A=	NP_001269472.1:p.Ser758=
NM_001282545.2:c.976A=	NP_001269474.1:p.Ser326=
NM_001282548.2:c.919A=	NP_001269477.1:p.Ser307=
NM_001282549.2:c.790A=	NP_001269478.1:p.Ser264=
NR_104212.2:n.2294A=
NR_104215.2:n.2237A=
NR_104216.2:n.1493A=