Canonical Allele Identifier: CA413149275
Gene: IQSEC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53241845T>A , CM000685.2:g.53241845T>A GRCh38
NC_000023.10:g.53271027T>A , CM000685.1:g.53271027T>A GRCh37
NC_000023.9:g.53287752T>A NCBI36
NG_021296.1:g.84496A>T
NG_021296.2:g.84506A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706952.1:c.3113A>T ENSP00000516672.1:p.Asn1038Ile
ENST00000638521.1:c.906A>T
ENST00000638869.1:c.415A>T
ENST00000639642.1:c.244A>T
ENST00000640005.1:c.17A>T ENSP00000491293.1:p.Asn6Ile
ENST00000640694.1:c.2954A>T ENSP00000492403.1:p.Asn985Ile
ENST00000642864.1:c.2954A>T MANE Select ENSP00000495726.1:p.Asn985Ile
ENST00000674510.1:c.2954A>T ENSP00000502054.1:p.Asn985Ile
ENST00000674761.1:n.1261A>T
ENST00000675719.1:c.2924A>T ENSP00000501927.1:p.Asn975Ile
ENST00000375365.2:c.2339A>T ENSP00000364514.2:p.Asn780Ile
ENST00000396435.7:c.2954A>T ENSP00000379712.3:p.Asn985Ile
NM_001111125.2:c.2954A>T NP_001104595.1:p.Asn985Ile
NM_015075.1:c.2339A>T NP_055890.1:p.Asn780Ile
XM_006724579.2:c.3050A>T XP_006724642.1:p.Asn1017Ile
XM_006724580.2:c.2339A>T XP_006724643.1:p.Asn780Ile
XM_006724581.2:c.3050A>T XP_006724644.1:p.Asn1017Ile
XM_006724582.2:c.3050A>T XP_006724645.1:p.Asn1017Ile
XM_006724583.2:c.3050A>T XP_006724646.1:p.Asn1017Ile
XM_006724584.2:c.3050A>T XP_006724647.1:p.Asn1017Ile
XM_011530772.1:c.2276A>T XP_011529074.1:p.Asn759Ile
XM_011530773.1:c.2243A>T XP_011529075.1:p.Asn748Ile
XM_011530774.1:c.3050A>T XP_011529076.1:p.Asn1017Ile
XM_011530775.1:c.3050A>T XP_011529077.1:p.Asn1017Ile
XM_011530776.1:c.3050A>T XP_011529078.1:p.Asn1017Ile
XM_011530777.1:c.3050A>T XP_011529079.1:p.Asn1017Ile
XR_938365.1:n.3277A>T
XM_006724579.3:c.3050A>T XP_006724642.1:p.Asn1017Ile
XM_006724580.3:c.2339A>T XP_006724643.1:p.Asn780Ile
XM_006724581.4:c.3050A>T XP_006724644.1:p.Asn1017Ile
XM_006724582.4:c.3050A>T XP_006724645.1:p.Asn1017Ile
XM_006724583.4:c.3050A>T XP_006724646.1:p.Asn1017Ile
XM_006724584.3:c.3050A>T XP_006724647.1:p.Asn1017Ile
XM_011530773.2:c.2243A>T XP_011529075.1:p.Asn748Ile
XM_011530774.3:c.3050A>T XP_011529076.1:p.Asn1017Ile
XM_011530776.2:c.3050A>T XP_011529078.1:p.Asn1017Ile
XM_011530777.2:c.3050A>T XP_011529079.1:p.Asn1017Ile
XM_017029359.2:c.2924A>T XP_016884848.1:p.Asn975Ile
XM_017029360.1:c.2456A>T XP_016884849.1:p.Asn819Ile
XR_938365.2:n.3271A>T
NM_001111125.3:c.2954A>T MANE Select NP_001104595.1:p.Asn985Ile
NM_015075.2:c.2339A>T NP_055890.1:p.Asn780Ile