Canonical Allele Identifier: CA2429777122

Gene: IQSEC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53255692_53255693delinsGC , CM000685.2:g.53255692_53255693delinsGC	GRCh38
NC_000023.10:g.53284874_53284875delinsGC , CM000685.1:g.53284874_53284875delinsGC	GRCh37
NC_000023.9:g.53301599_53301600delinsGC	NCBI36
NG_021296.1:g.70648_70649delinsGC
NG_021296.2:g.70658_70659delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.1158+107_1158+108delinsGC	ENSP00000516672.1:n.1158+107_1158+108delinsGC
ENST00000638630.1:c.288+107_288+108delinsGC	ENSP00000492390.1:n.288+107_288+108delinsGC
ENST00000640694.1:c.999+107_999+108delinsGC	ENSP00000492403.1:n.999+107_999+108delinsGC
ENST00000642864.1:c.999+107_999+108delinsGC MANE Select	ENSP00000495726.1:n.999+107_999+108delinsGC
ENST00000674510.1:c.999+107_999+108delinsGC	ENSP00000502054.1:n.999+107_999+108delinsGC
ENST00000675719.1:c.969+107_969+108delinsGC	ENSP00000501927.1:n.969+107_969+108delinsGC
ENST00000375365.2:c.384+107_384+108delinsGC	ENSP00000364514.2:n.384+107_384+108delinsGC
ENST00000396435.7:c.999+107_999+108delinsGC	ENSP00000379712.3:n.999+107_999+108delinsGC
NM_001111125.2:c.999+107_999+108delinsGC	NP_001104595.1:n.999+107_999+108delinsGC
NM_015075.1:c.384+107_384+108delinsGC	NP_055890.1:n.384+107_384+108delinsGC
XM_006724579.2:c.1095+107_1095+108delinsGC	XP_006724642.1:n.1095+107_1095+108delinsGC
XM_006724580.2:c.384+107_384+108delinsGC	XP_006724643.1:n.384+107_384+108delinsGC
XM_006724581.2:c.1095+107_1095+108delinsGC	XP_006724644.1:n.1095+107_1095+108delinsGC
XM_006724582.2:c.1095+107_1095+108delinsGC	XP_006724645.1:n.1095+107_1095+108delinsGC
XM_006724583.2:c.1095+107_1095+108delinsGC	XP_006724646.1:n.1095+107_1095+108delinsGC
XM_006724584.2:c.1095+107_1095+108delinsGC	XP_006724647.1:n.1095+107_1095+108delinsGC
XM_011530772.1:c.321+107_321+108delinsGC	XP_011529074.1:n.321+107_321+108delinsGC
XM_011530773.1:c.288+107_288+108delinsGC	XP_011529075.1:n.288+107_288+108delinsGC
XM_011530774.1:c.1095+107_1095+108delinsGC	XP_011529076.1:n.1095+107_1095+108delinsGC
XM_011530775.1:c.1095+107_1095+108delinsGC	XP_011529077.1:n.1095+107_1095+108delinsGC
XM_011530776.1:c.1095+107_1095+108delinsGC	XP_011529078.1:n.1095+107_1095+108delinsGC
XM_011530777.1:c.1095+107_1095+108delinsGC	XP_011529079.1:n.1095+107_1095+108delinsGC
XR_938365.1:n.1322+107_1322+108delinsGC
XM_006724579.3:c.1095+107_1095+108delinsGC	XP_006724642.1:n.1095+107_1095+108delinsGC
XM_006724580.3:c.384+107_384+108delinsGC	XP_006724643.1:n.384+107_384+108delinsGC
XM_006724581.4:c.1095+107_1095+108delinsGC	XP_006724644.1:n.1095+107_1095+108delinsGC
XM_006724582.4:c.1095+107_1095+108delinsGC	XP_006724645.1:n.1095+107_1095+108delinsGC
XM_006724583.4:c.1095+107_1095+108delinsGC	XP_006724646.1:n.1095+107_1095+108delinsGC
XM_006724584.3:c.1095+107_1095+108delinsGC	XP_006724647.1:n.1095+107_1095+108delinsGC
XM_011530773.2:c.288+107_288+108delinsGC	XP_011529075.1:n.288+107_288+108delinsGC
XM_011530774.3:c.1095+107_1095+108delinsGC	XP_011529076.1:n.1095+107_1095+108delinsGC
XM_011530776.2:c.1095+107_1095+108delinsGC	XP_011529078.1:n.1095+107_1095+108delinsGC
XM_011530777.2:c.1095+107_1095+108delinsGC	XP_011529079.1:n.1095+107_1095+108delinsGC
XM_017029359.2:c.969+107_969+108delinsGC	XP_016884848.1:n.969+107_969+108delinsGC
XM_017029360.1:c.501+107_501+108delinsGC	XP_016884849.1:n.501+107_501+108delinsGC
XR_938365.2:n.1316+107_1316+108delinsGC
NM_001111125.3:c.999+107_999+108delinsGC MANE Select	NP_001104595.1:n.999+107_999+108delinsGC
NM_015075.2:c.384+107_384+108delinsGC	NP_055890.1:n.384+107_384+108delinsGC