Canonical Allele Identifier: CA1327076742

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214792434_214792435delinsCT , CM000664.2:g.214792434_214792435delinsCT	GRCh38
NC_000002.11:g.215657158_215657159delinsCT , CM000664.1:g.215657158_215657159delinsCT	GRCh37
NC_000002.10:g.215365403_215365404delinsCT	NCBI36
NG_012047.2:g.22270_22271delinsAG
NG_012047.3:g.22277_22278delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.226_227delinsAG MANE Select	ENSP00000260947.4:p.Ser76=
ENST00000421162.2:c.215+4626_215+4627delinsAG	ENSP00000392245.2:n.215+4626_215+4627delinsAG
ENST00000613192.2:c.158+16977_158+16978delinsAG	ENSP00000483275.2:n.158+16977_158+16978delinsAG
ENST00000613374.5:c.158+16977_158+16978delinsAG	ENSP00000484464.1:n.158+16977_158+16978delinsAG
ENST00000613706.5:c.226_227delinsAG	ENSP00000484976.2:p.Ser76=
ENST00000617164.5:c.169_170delinsAG	ENSP00000480470.1:p.Ser57=
ENST00000619009.5:c.226_227delinsAG	ENSP00000482293.1:p.Ser76=
ENST00000650978.1:c.68_69delinsAG
ENST00000260947.8:c.226_227delinsAG	ENSP00000260947.4:p.Ser76=
ENST00000421162.1:c.215+4626_215+4627delinsAG	ENSP00000392245.1:n.215+4626_215+4627delinsAG
ENST00000455743.5:c.215+4626_215+4627delinsAG	ENSP00000412186.1:n.215+4626_215+4627delinsAG
ENST00000471787.1:n.260-10926_260-10925delinsAG
ENST00000613192.1:c.73+16977_73+16978delinsAG	ENSP00000483275.1:n.73+16977_73+16978delinsAG
ENST00000613374.4:c.158+16977_158+16978delinsAG	ENSP00000484464.1:n.158+16977_158+16978delinsAG
ENST00000613706.4:c.215+4626_215+4627delinsAG	ENSP00000484976.1:n.215+4626_215+4627delinsAG
ENST00000617164.4:c.169_170delinsAG	ENSP00000480470.1:p.Ser57=
ENST00000619009.4:c.226_227delinsAG	ENSP00000482293.1:p.Ser76=
ENST00000620057.4:c.226_227delinsAG	ENSP00000481988.1:p.Ser76=
NM_000465.3:c.226_227delinsAG	NP_000456.2:p.Ser76=
NM_001282543.1:c.169_170delinsAG	NP_001269472.1:p.Ser57=
NM_001282545.1:c.215+4626_215+4627delinsAG	NP_001269474.1:n.215+4626_215+4627delinsAG
NM_001282548.1:c.158+16977_158+16978delinsAG	NP_001269477.1:n.158+16977_158+16978delinsAG
NM_001282549.1:c.226_227delinsAG	NP_001269478.1:p.Ser76=
NR_104212.1:n.357+4626_357+4627delinsAG
NR_104215.1:n.301-10926_301-10925delinsAG
NR_104216.1:n.368_369delinsAG
XM_011511567.1:c.172_173delinsAG	XP_011509869.1:p.Ser58=
XM_011511568.1:c.226_227delinsAG	XP_011509870.1:p.Ser76=
XM_017004613.1:c.325_326delinsAG	XP_016860102.1:p.Ser109=
XM_017004614.1:c.325_326delinsAG	XP_016860103.1:p.Ser109=
XR_002959322.1:n.416_417delinsAG
NM_000465.4:c.226_227delinsAG MANE Select	NP_000456.2:p.Ser76=
NM_001282543.2:c.169_170delinsAG	NP_001269472.1:p.Ser57=
NM_001282545.2:c.215+4626_215+4627delinsAG	NP_001269474.1:n.215+4626_215+4627delinsAG
NM_001282548.2:c.158+16977_158+16978delinsAG	NP_001269477.1:n.158+16977_158+16978delinsAG
NM_001282549.2:c.226_227delinsAG	NP_001269478.1:p.Ser76=
NR_104212.2:n.329+4626_329+4627delinsAG
NR_104215.2:n.273-10926_273-10925delinsAG
NR_104216.2:n.340_341delinsAG