Canonical Allele Identifier: CA2429775636

Gene: IQSEC2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53250762_53250763delinsTC , CM000685.2:g.53250762_53250763delinsTC	GRCh38
NC_000023.10:g.53279944_53279945delinsTC , CM000685.1:g.53279944_53279945delinsTC	GRCh37
NC_000023.9:g.53296669_53296670delinsTC	NCBI36
NG_021296.1:g.75578_75579delinsGA
NG_021296.2:g.75588_75589delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000706952.1:c.1972_1973delinsGA	ENSP00000516672.1:p.Asp658=
ENST00000640694.1:c.1813_1814delinsGA	ENSP00000492403.1:p.Asp605=
ENST00000642864.1:c.1813_1814delinsGA MANE Select	ENSP00000495726.1:p.Asp605=
ENST00000674510.1:c.1813_1814delinsGA	ENSP00000502054.1:p.Asp605=
ENST00000675719.1:c.1783_1784delinsGA	ENSP00000501927.1:p.Asp595=
ENST00000375365.2:c.1198_1199delinsGA	ENSP00000364514.2:p.Asp400=
ENST00000396435.7:c.1813_1814delinsGA	ENSP00000379712.3:p.Asp605=
NM_001111125.2:c.1813_1814delinsGA	NP_001104595.1:p.Asp605=
NM_015075.1:c.1198_1199delinsGA	NP_055890.1:p.Asp400=
XM_006724579.2:c.1909_1910delinsGA	XP_006724642.1:p.Asp637=
XM_006724580.2:c.1198_1199delinsGA	XP_006724643.1:p.Asp400=
XM_006724581.2:c.1909_1910delinsGA	XP_006724644.1:p.Asp637=
XM_006724582.2:c.1909_1910delinsGA	XP_006724645.1:p.Asp637=
XM_006724583.2:c.1909_1910delinsGA	XP_006724646.1:p.Asp637=
XM_006724584.2:c.1909_1910delinsGA	XP_006724647.1:p.Asp637=
XM_011530772.1:c.1135_1136delinsGA	XP_011529074.1:p.Asp379=
XM_011530773.1:c.1102_1103delinsGA	XP_011529075.1:p.Asp368=
XM_011530774.1:c.1909_1910delinsGA	XP_011529076.1:p.Asp637=
XM_011530775.1:c.1909_1910delinsGA	XP_011529077.1:p.Asp637=
XM_011530776.1:c.1909_1910delinsGA	XP_011529078.1:p.Asp637=
XM_011530777.1:c.1909_1910delinsGA	XP_011529079.1:p.Asp637=
XR_938365.1:n.2136_2137delinsGA
XM_006724579.3:c.1909_1910delinsGA	XP_006724642.1:p.Asp637=
XM_006724580.3:c.1198_1199delinsGA	XP_006724643.1:p.Asp400=
XM_006724581.4:c.1909_1910delinsGA	XP_006724644.1:p.Asp637=
XM_006724582.4:c.1909_1910delinsGA	XP_006724645.1:p.Asp637=
XM_006724583.4:c.1909_1910delinsGA	XP_006724646.1:p.Asp637=
XM_006724584.3:c.1909_1910delinsGA	XP_006724647.1:p.Asp637=
XM_011530773.2:c.1102_1103delinsGA	XP_011529075.1:p.Asp368=
XM_011530774.3:c.1909_1910delinsGA	XP_011529076.1:p.Asp637=
XM_011530776.2:c.1909_1910delinsGA	XP_011529078.1:p.Asp637=
XM_011530777.2:c.1909_1910delinsGA	XP_011529079.1:p.Asp637=
XM_017029359.2:c.1783_1784delinsGA	XP_016884848.1:p.Asp595=
XM_017029360.1:c.1315_1316delinsGA	XP_016884849.1:p.Asp439=
XR_938365.2:n.2130_2131delinsGA
NM_001111125.3:c.1813_1814delinsGA MANE Select	NP_001104595.1:p.Asp605=
NM_015075.2:c.1198_1199delinsGA	NP_055890.1:p.Asp400=