Canonical Allele Identifier: CA1133162622

Gene: IQSEC2

Linked Data

• dbSNP Id: rs2074331940
• gnomAD v3: X-53247942-G-GAT
• gnomAD v4: X-53247942-G-GAT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53247944_53247945dup , CM000685.2:g.53247944_53247945dup	GRCh38
NC_000023.10:g.53277126_53277127dup , CM000685.1:g.53277126_53277127dup	GRCh37
NC_000023.9:g.53293851_53293852dup	NCBI36
NG_021296.1:g.78397_78398dup
NG_021296.2:g.78407_78408dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.2741+170_2741+171dup	ENSP00000516672.1:n.2741+170_2741+171dup
ENST00000638521.1:c.534+170_534+171dup
ENST00000638869.1:c.43+170_43+171dup
ENST00000640694.1:c.2582+170_2582+171dup	ENSP00000492403.1:n.2582+170_2582+171dup
ENST00000642864.1:c.2582+170_2582+171dup MANE Select	ENSP00000495726.1:n.2582+170_2582+171dup
ENST00000674510.1:c.2582+170_2582+171dup	ENSP00000502054.1:n.2582+170_2582+171dup
ENST00000674761.1:n.333+170_333+171dup
ENST00000675719.1:c.2552+170_2552+171dup	ENSP00000501927.1:n.2552+170_2552+171dup
ENST00000375365.2:c.1967+170_1967+171dup	ENSP00000364514.2:n.1967+170_1967+171dup
ENST00000396435.7:c.2582+170_2582+171dup	ENSP00000379712.3:n.2582+170_2582+171dup
NM_001111125.2:c.2582+170_2582+171dup	NP_001104595.1:n.2582+170_2582+171dup
NM_015075.1:c.1967+170_1967+171dup	NP_055890.1:n.1967+170_1967+171dup
XM_006724579.2:c.2678+170_2678+171dup	XP_006724642.1:n.2678+170_2678+171dup
XM_006724580.2:c.1967+170_1967+171dup	XP_006724643.1:n.1967+170_1967+171dup
XM_006724581.2:c.2678+170_2678+171dup	XP_006724644.1:n.2678+170_2678+171dup
XM_006724582.2:c.2678+170_2678+171dup	XP_006724645.1:n.2678+170_2678+171dup
XM_006724583.2:c.2678+170_2678+171dup	XP_006724646.1:n.2678+170_2678+171dup
XM_006724584.2:c.2678+170_2678+171dup	XP_006724647.1:n.2678+170_2678+171dup
XM_011530772.1:c.1904+170_1904+171dup	XP_011529074.1:n.1904+170_1904+171dup
XM_011530773.1:c.1871+170_1871+171dup	XP_011529075.1:n.1871+170_1871+171dup
XM_011530774.1:c.2678+170_2678+171dup	XP_011529076.1:n.2678+170_2678+171dup
XM_011530775.1:c.2678+170_2678+171dup	XP_011529077.1:n.2678+170_2678+171dup
XM_011530776.1:c.2678+170_2678+171dup	XP_011529078.1:n.2678+170_2678+171dup
XM_011530777.1:c.2678+170_2678+171dup	XP_011529079.1:n.2678+170_2678+171dup
XR_938365.1:n.2905+170_2905+171dup
XM_006724579.3:c.2678+170_2678+171dup	XP_006724642.1:n.2678+170_2678+171dup
XM_006724580.3:c.1967+170_1967+171dup	XP_006724643.1:n.1967+170_1967+171dup
XM_006724581.4:c.2678+170_2678+171dup	XP_006724644.1:n.2678+170_2678+171dup
XM_006724582.4:c.2678+170_2678+171dup	XP_006724645.1:n.2678+170_2678+171dup
XM_006724583.4:c.2678+170_2678+171dup	XP_006724646.1:n.2678+170_2678+171dup
XM_006724584.3:c.2678+170_2678+171dup	XP_006724647.1:n.2678+170_2678+171dup
XM_011530773.2:c.1871+170_1871+171dup	XP_011529075.1:n.1871+170_1871+171dup
XM_011530774.3:c.2678+170_2678+171dup	XP_011529076.1:n.2678+170_2678+171dup
XM_011530776.2:c.2678+170_2678+171dup	XP_011529078.1:n.2678+170_2678+171dup
XM_011530777.2:c.2678+170_2678+171dup	XP_011529079.1:n.2678+170_2678+171dup
XM_017029359.2:c.2552+170_2552+171dup	XP_016884848.1:n.2552+170_2552+171dup
XM_017029360.1:c.2084+170_2084+171dup	XP_016884849.1:n.2084+170_2084+171dup
XR_938365.2:n.2899+170_2899+171dup
NM_001111125.3:c.2582+170_2582+171dup MANE Select	NP_001104595.1:n.2582+170_2582+171dup
NM_015075.2:c.1967+170_1967+171dup	NP_055890.1:n.1967+170_1967+171dup