Canonical Allele Identifier: CA641903991

Gene: IQSEC2

Linked Data

• dbSNP Id: rs1556863417
• gnomAD v2: X-53280114-T-TG
• gnomAD v4: X-53250932-T-TG
• MyVariant Identifiers: chrX:g.53280114_53280115insG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53250934dup , CM000685.2:g.53250934dup	GRCh38
NC_000023.10:g.53280116dup , CM000685.1:g.53280116dup	GRCh37
NC_000023.9:g.53296841dup	NCBI36
NG_021296.1:g.75408dup
NG_021296.2:g.75418dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000706952.1:c.1802dup	ENSP00000516672.1:p.Ala602SerfsTer19
ENST00000640694.1:c.1643dup	ENSP00000492403.1:p.Ala549SerfsTer19
ENST00000642864.1:c.1643dup MANE Select	ENSP00000495726.1:p.Ala549SerfsTer19
ENST00000674510.1:c.1643dup	ENSP00000502054.1:p.Ala549SerfsTer19
ENST00000675719.1:c.1613dup	ENSP00000501927.1:p.Ala539SerfsTer19
ENST00000375365.2:c.1028dup	ENSP00000364514.2:p.Ala344SerfsTer19
ENST00000396435.7:c.1643dup	ENSP00000379712.3:p.Ala549SerfsTer19
NM_001111125.2:c.1643dup	NP_001104595.1:p.Ala549SerfsTer19
NM_015075.1:c.1028dup	NP_055890.1:p.Ala344SerfsTer19
XM_006724579.2:c.1739dup	XP_006724642.1:p.Ala581SerfsTer19
XM_006724580.2:c.1028dup	XP_006724643.1:p.Ala344SerfsTer19
XM_006724581.2:c.1739dup	XP_006724644.1:p.Ala581SerfsTer19
XM_006724582.2:c.1739dup	XP_006724645.1:p.Ala581SerfsTer19
XM_006724583.2:c.1739dup	XP_006724646.1:p.Ala581SerfsTer19
XM_006724584.2:c.1739dup	XP_006724647.1:p.Ala581SerfsTer19
XM_011530772.1:c.965dup	XP_011529074.1:p.Ala323SerfsTer19
XM_011530773.1:c.932dup	XP_011529075.1:p.Ala312SerfsTer19
XM_011530774.1:c.1739dup	XP_011529076.1:p.Ala581SerfsTer19
XM_011530775.1:c.1739dup	XP_011529077.1:p.Ala581SerfsTer19
XM_011530776.1:c.1739dup	XP_011529078.1:p.Ala581SerfsTer19
XM_011530777.1:c.1739dup	XP_011529079.1:p.Ala581SerfsTer19
XR_938365.1:n.1966dup
XM_006724579.3:c.1739dup	XP_006724642.1:p.Ala581SerfsTer19
XM_006724580.3:c.1028dup	XP_006724643.1:p.Ala344SerfsTer19
XM_006724581.4:c.1739dup	XP_006724644.1:p.Ala581SerfsTer19
XM_006724582.4:c.1739dup	XP_006724645.1:p.Ala581SerfsTer19
XM_006724583.4:c.1739dup	XP_006724646.1:p.Ala581SerfsTer19
XM_006724584.3:c.1739dup	XP_006724647.1:p.Ala581SerfsTer19
XM_011530773.2:c.932dup	XP_011529075.1:p.Ala312SerfsTer19
XM_011530774.3:c.1739dup	XP_011529076.1:p.Ala581SerfsTer19
XM_011530776.2:c.1739dup	XP_011529078.1:p.Ala581SerfsTer19
XM_011530777.2:c.1739dup	XP_011529079.1:p.Ala581SerfsTer19
XM_017029359.2:c.1613dup	XP_016884848.1:p.Ala539SerfsTer19
XM_017029360.1:c.1145dup	XP_016884849.1:p.Ala383SerfsTer19
XR_938365.2:n.1960dup
NM_001111125.3:c.1643dup MANE Select	NP_001104595.1:p.Ala549SerfsTer19
NM_015075.2:c.1028dup	NP_055890.1:p.Ala344SerfsTer19