Canonical Allele Identifier: CA2662971964

Gene: BARD1

Linked Data

• gnomAD v4: 2-214792160-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214792160_214792161insC , CM000664.2:g.214792160_214792161insC	GRCh38
NC_000002.11:g.215656884_215656885insC , CM000664.1:g.215656884_215656885insC	GRCh37
NC_000002.10:g.215365129_215365130insC	NCBI36
NG_012047.2:g.22544_22545insG
NG_012047.3:g.22551_22552insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000260947.9:c.364+136_364+137insG MANE Select	ENSP00000260947.4:n.364+136_364+137insG
ENST00000421162.2:c.215+4900_215+4901insG	ENSP00000392245.2:n.215+4900_215+4901insG...
ENST00000613192.2:c.158+17251_158+17252insG	ENSP00000483275.2:n.158+17251_158+17252in...
ENST00000613374.5:c.158+17251_158+17252insG	ENSP00000484464.1:n.158+17251_158+17252in...
ENST00000613706.5:c.364+136_364+137insG	ENSP00000484976.2:n.364+136_364+137insG
ENST00000617164.5:c.307+136_307+137insG	ENSP00000480470.1:n.307+136_307+137insG
ENST00000619009.5:c.364+136_364+137insG	ENSP00000482293.1:n.364+136_364+137insG
ENST00000650978.1:c.206+136_206+137insG
ENST00000260947.8:c.364+136_364+137insG	ENSP00000260947.4:n.364+136_364+137insG
ENST00000421162.1:c.215+4900_215+4901insG	ENSP00000392245.1:n.215+4900_215+4901insG...
ENST00000455743.5:c.215+4900_215+4901insG	ENSP00000412186.1:n.215+4900_215+4901insG...
ENST00000471787.1:n.260-10652_260-10651insG
ENST00000613192.1:c.73+17251_73+17252insG	ENSP00000483275.1:n.73+17251_73+17252insG...
ENST00000613374.4:c.158+17251_158+17252insG	ENSP00000484464.1:n.158+17251_158+17252in...
ENST00000613706.4:c.215+4900_215+4901insG	ENSP00000484976.1:n.215+4900_215+4901insG...
ENST00000617164.4:c.307+136_307+137insG	ENSP00000480470.1:n.307+136_307+137insG
ENST00000619009.4:c.364+136_364+137insG	ENSP00000482293.1:n.364+136_364+137insG
ENST00000620057.4:c.364+136_364+137insG	ENSP00000481988.1:n.364+136_364+137insG
NM_000465.3:c.364+136_364+137insG	NP_000456.2:n.364+136_364+137insG
NM_001282543.1:c.307+136_307+137insG	NP_001269472.1:n.307+136_307+137insG
NM_001282545.1:c.215+4900_215+4901insG	NP_001269474.1:n.215+4900_215+4901insG
NM_001282548.1:c.158+17251_158+17252insG	NP_001269477.1:n.158+17251_158+17252insG
NM_001282549.1:c.364+136_364+137insG	NP_001269478.1:n.364+136_364+137insG
NR_104212.1:n.357+4900_357+4901insG
NR_104215.1:n.301-10652_301-10651insG
NR_104216.1:n.506+136_506+137insG
XM_011511567.1:c.310+136_310+137insG	XP_011509869.1:n.310+136_310+137insG
XM_011511568.1:c.364+136_364+137insG	XP_011509870.1:n.364+136_364+137insG
XM_017004613.1:c.463+136_463+137insG	XP_016860102.1:n.463+136_463+137insG
XM_017004614.1:c.463+136_463+137insG	XP_016860103.1:n.463+136_463+137insG
XR_002959322.1:n.554+136_554+137insG
NM_000465.4:c.364+136_364+137insG MANE Select	NP_000456.2:n.364+136_364+137insG
NM_001282543.2:c.307+136_307+137insG	NP_001269472.1:n.307+136_307+137insG
NM_001282545.2:c.215+4900_215+4901insG	NP_001269474.1:n.215+4900_215+4901insG
NM_001282548.2:c.158+17251_158+17252insG	NP_001269477.1:n.158+17251_158+17252insG
NM_001282549.2:c.364+136_364+137insG	NP_001269478.1:n.364+136_364+137insG
NR_104212.2:n.329+4900_329+4901insG
NR_104215.2:n.273-10652_273-10651insG
NR_104216.2:n.478+136_478+137insG