Canonical Allele Identifier: CA1327076705

Gene: BARD1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214792387_214792388delinsTC , CM000664.2:g.214792387_214792388delinsTC	GRCh38
NC_000002.11:g.215657111_215657112delinsTC , CM000664.1:g.215657111_215657112delinsTC	GRCh37
NC_000002.10:g.215365356_215365357delinsTC	NCBI36
NG_012047.2:g.22317_22318delinsGA
NG_012047.3:g.22324_22325delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260947.9:c.273_274delinsGA MANE Select	ENSP00000260947.4:p.Trp91=
ENST00000421162.2:c.215+4673_215+4674delinsGA	ENSP00000392245.2:n.215+4673_215+4674delinsGA
ENST00000613192.2:c.158+17024_158+17025delinsGA	ENSP00000483275.2:n.158+17024_158+17025delinsGA
ENST00000613374.5:c.158+17024_158+17025delinsGA	ENSP00000484464.1:n.158+17024_158+17025delinsGA
ENST00000613706.5:c.273_274delinsGA	ENSP00000484976.2:p.Trp91=
ENST00000617164.5:c.216_217delinsGA	ENSP00000480470.1:p.Trp72=
ENST00000619009.5:c.273_274delinsGA	ENSP00000482293.1:p.Trp91=
ENST00000650978.1:c.115_116delinsGA
ENST00000260947.8:c.273_274delinsGA	ENSP00000260947.4:p.Trp91=
ENST00000421162.1:c.215+4673_215+4674delinsGA	ENSP00000392245.1:n.215+4673_215+4674delinsGA
ENST00000455743.5:c.215+4673_215+4674delinsGA	ENSP00000412186.1:n.215+4673_215+4674delinsGA
ENST00000471787.1:n.260-10879_260-10878delinsGA
ENST00000613192.1:c.73+17024_73+17025delinsGA	ENSP00000483275.1:n.73+17024_73+17025delinsGA
ENST00000613374.4:c.158+17024_158+17025delinsGA	ENSP00000484464.1:n.158+17024_158+17025delinsGA
ENST00000613706.4:c.215+4673_215+4674delinsGA	ENSP00000484976.1:n.215+4673_215+4674delinsGA
ENST00000617164.4:c.216_217delinsGA	ENSP00000480470.1:p.Trp72=
ENST00000619009.4:c.273_274delinsGA	ENSP00000482293.1:p.Trp91=
ENST00000620057.4:c.273_274delinsGA	ENSP00000481988.1:p.Trp91=
NM_000465.3:c.273_274delinsGA	NP_000456.2:p.Trp91=
NM_001282543.1:c.216_217delinsGA	NP_001269472.1:p.Trp72=
NM_001282545.1:c.215+4673_215+4674delinsGA	NP_001269474.1:n.215+4673_215+4674delinsGA
NM_001282548.1:c.158+17024_158+17025delinsGA	NP_001269477.1:n.158+17024_158+17025delinsGA
NM_001282549.1:c.273_274delinsGA	NP_001269478.1:p.Trp91=
NR_104212.1:n.357+4673_357+4674delinsGA
NR_104215.1:n.301-10879_301-10878delinsGA
NR_104216.1:n.415_416delinsGA
XM_011511567.1:c.219_220delinsGA	XP_011509869.1:p.Trp73=
XM_011511568.1:c.273_274delinsGA	XP_011509870.1:p.Trp91=
XM_017004613.1:c.372_373delinsGA	XP_016860102.1:p.Trp124=
XM_017004614.1:c.372_373delinsGA	XP_016860103.1:p.Trp124=
XR_002959322.1:n.463_464delinsGA
NM_000465.4:c.273_274delinsGA MANE Select	NP_000456.2:p.Trp91=
NM_001282543.2:c.216_217delinsGA	NP_001269472.1:p.Trp72=
NM_001282545.2:c.215+4673_215+4674delinsGA	NP_001269474.1:n.215+4673_215+4674delinsGA
NM_001282548.2:c.158+17024_158+17025delinsGA	NP_001269477.1:n.158+17024_158+17025delinsGA
NM_001282549.2:c.273_274delinsGA	NP_001269478.1:p.Trp91=
NR_104212.2:n.329+4673_329+4674delinsGA
NR_104215.2:n.273-10879_273-10878delinsGA
NR_104216.2:n.387_388delinsGA