Canonical Allele Identifier: CA1327078939

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214797081_214797082delinsTC , CM000664.2:g.214797081_214797082delinsTC	GRCh38
NC_000002.11:g.215661805_215661806delinsTC , CM000664.1:g.215661805_215661806delinsTC	GRCh37
NC_000002.10:g.215370050_215370051delinsTC	NCBI36
NG_012047.2:g.17623_17624delinsGA
NG_012047.3:g.17630_17631delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.194_195delinsGA MANE Select	ENSP00000260947.4:p.Gly65=
ENST00000421162.2:c.194_195delinsGA	ENSP00000392245.2:p.Gly65=
ENST00000613192.2:c.158+12330_158+12331delinsGA	ENSP00000483275.2:n.158+12330_158+12331delinsGA
ENST00000613374.5:c.158+12330_158+12331delinsGA	ENSP00000484464.1:n.158+12330_158+12331delinsGA
ENST00000613706.5:c.194_195delinsGA	ENSP00000484976.2:p.Gly65=
ENST00000617164.5:c.159-4637_159-4636delinsGA	ENSP00000480470.1:n.159-4637_159-4636delinsGA
ENST00000619009.5:c.194_195delinsGA	ENSP00000482293.1:p.Gly65=
ENST00000650978.1:c.36_37delinsGA
ENST00000260947.8:c.194_195delinsGA	ENSP00000260947.4:p.Gly65=
ENST00000421162.1:c.194_195delinsGA	ENSP00000392245.1:p.Gly65=
ENST00000455743.5:c.194_195delinsGA	ENSP00000412186.1:p.Gly65=
ENST00000471787.1:n.259+12330_259+12331delinsGA
ENST00000479904.1:n.285_286delinsGA
ENST00000613192.1:c.73+12330_73+12331delinsGA	ENSP00000483275.1:n.73+12330_73+12331delinsGA
ENST00000613374.4:c.158+12330_158+12331delinsGA	ENSP00000484464.1:n.158+12330_158+12331delinsGA
ENST00000613706.4:c.194_195delinsGA	ENSP00000484976.1:p.Gly65=
ENST00000617164.4:c.159-4637_159-4636delinsGA	ENSP00000480470.1:n.159-4637_159-4636delinsGA
ENST00000619009.4:c.194_195delinsGA	ENSP00000482293.1:p.Gly65=
ENST00000620057.4:c.194_195delinsGA	ENSP00000481988.1:p.Gly65=
NM_000465.3:c.194_195delinsGA	NP_000456.2:p.Gly65=
NM_001282543.1:c.159-4637_159-4636delinsGA	NP_001269472.1:n.159-4637_159-4636delinsGA
NM_001282545.1:c.194_195delinsGA	NP_001269474.1:p.Gly65=
NM_001282548.1:c.158+12330_158+12331delinsGA	NP_001269477.1:n.158+12330_158+12331delinsGA
NM_001282549.1:c.194_195delinsGA	NP_001269478.1:p.Gly65=
NR_104212.1:n.336_337delinsGA
NR_104215.1:n.300+12330_300+12331delinsGA
NR_104216.1:n.336_337delinsGA
XM_011511567.1:c.140_141delinsGA	XP_011509869.1:p.Gly47=
XM_011511568.1:c.194_195delinsGA	XP_011509870.1:p.Gly65=
XM_017004613.1:c.194_195delinsGA	XP_016860102.1:p.Gly65=
XM_017004614.1:c.194_195delinsGA	XP_016860103.1:p.Gly65=
XR_002959322.1:n.285_286delinsGA
NM_000465.4:c.194_195delinsGA MANE Select	NP_000456.2:p.Gly65=
NM_001282543.2:c.159-4637_159-4636delinsGA	NP_001269472.1:n.159-4637_159-4636delinsGA
NM_001282545.2:c.194_195delinsGA	NP_001269474.1:p.Gly65=
NM_001282548.2:c.158+12330_158+12331delinsGA	NP_001269477.1:n.158+12330_158+12331delinsGA
NM_001282549.2:c.194_195delinsGA	NP_001269478.1:p.Gly65=
NR_104212.2:n.308_309delinsGA
NR_104215.2:n.272+12330_272+12331delinsGA
NR_104216.2:n.308_309delinsGA