Canonical Allele Identifier: CA2429777197

Gene: IQSEC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53255935_53255936delinsCA , CM000685.2:g.53255935_53255936delinsCA	GRCh38
NC_000023.10:g.53285117_53285118delinsCA , CM000685.1:g.53285117_53285118delinsCA	GRCh37
NC_000023.9:g.53301842_53301843delinsCA	NCBI36
NG_021296.1:g.70405_70406delinsTG
NG_021296.2:g.70415_70416delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.1022_1023delinsTG	ENSP00000516672.1:p.Val341=
ENST00000638630.1:c.152_153delinsTG	ENSP00000492390.1:p.Val51=
ENST00000640694.1:c.863_864delinsTG	ENSP00000492403.1:p.Val288=
ENST00000642864.1:c.863_864delinsTG MANE Select	ENSP00000495726.1:p.Val288=
ENST00000674510.1:c.863_864delinsTG	ENSP00000502054.1:p.Val288=
ENST00000675719.1:c.833_834delinsTG	ENSP00000501927.1:p.Val278=
ENST00000375365.2:c.248_249delinsTG	ENSP00000364514.2:p.Val83=
ENST00000396435.7:c.863_864delinsTG	ENSP00000379712.3:p.Val288=
NM_001111125.2:c.863_864delinsTG	NP_001104595.1:p.Val288=
NM_015075.1:c.248_249delinsTG	NP_055890.1:p.Val83=
XM_006724579.2:c.959_960delinsTG	XP_006724642.1:p.Val320=
XM_006724580.2:c.248_249delinsTG	XP_006724643.1:p.Val83=
XM_006724581.2:c.959_960delinsTG	XP_006724644.1:p.Val320=
XM_006724582.2:c.959_960delinsTG	XP_006724645.1:p.Val320=
XM_006724583.2:c.959_960delinsTG	XP_006724646.1:p.Val320=
XM_006724584.2:c.959_960delinsTG	XP_006724647.1:p.Val320=
XM_011530772.1:c.185_186delinsTG	XP_011529074.1:p.Val62=
XM_011530773.1:c.152_153delinsTG	XP_011529075.1:p.Val51=
XM_011530774.1:c.959_960delinsTG	XP_011529076.1:p.Val320=
XM_011530775.1:c.959_960delinsTG	XP_011529077.1:p.Val320=
XM_011530776.1:c.959_960delinsTG	XP_011529078.1:p.Val320=
XM_011530777.1:c.959_960delinsTG	XP_011529079.1:p.Val320=
XR_938365.1:n.1186_1187delinsTG
XM_006724579.3:c.959_960delinsTG	XP_006724642.1:p.Val320=
XM_006724580.3:c.248_249delinsTG	XP_006724643.1:p.Val83=
XM_006724581.4:c.959_960delinsTG	XP_006724644.1:p.Val320=
XM_006724582.4:c.959_960delinsTG	XP_006724645.1:p.Val320=
XM_006724583.4:c.959_960delinsTG	XP_006724646.1:p.Val320=
XM_006724584.3:c.959_960delinsTG	XP_006724647.1:p.Val320=
XM_011530773.2:c.152_153delinsTG	XP_011529075.1:p.Val51=
XM_011530774.3:c.959_960delinsTG	XP_011529076.1:p.Val320=
XM_011530776.2:c.959_960delinsTG	XP_011529078.1:p.Val320=
XM_011530777.2:c.959_960delinsTG	XP_011529079.1:p.Val320=
XM_017029359.2:c.833_834delinsTG	XP_016884848.1:p.Val278=
XM_017029360.1:c.365_366delinsTG	XP_016884849.1:p.Val122=
XR_938365.2:n.1180_1181delinsTG
NM_001111125.3:c.863_864delinsTG MANE Select	NP_001104595.1:p.Val288=
NM_015075.2:c.248_249delinsTG	NP_055890.1:p.Val83=