Canonical Allele Identifier: CA413149643

Gene: IQSEC2

Linked Data

• MyVariant Identifiers: chrX:g.53271067G>C (hg19) ; chrX:g.53241885G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53241885G>C , CM000685.2:g.53241885G>C	GRCh38
NC_000023.10:g.53271067G>C , CM000685.1:g.53271067G>C	GRCh37
NC_000023.9:g.53287792G>C	NCBI36
NG_021296.1:g.84456C>G
NG_021296.2:g.84466C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706952.1:c.3073C>G	ENSP00000516672.1:p.Leu1025Val
ENST00000638521.1:c.866C>G
ENST00000638869.1:c.375C>G
ENST00000639642.1:c.204C>G
ENST00000640694.1:c.2914C>G	ENSP00000492403.1:p.Leu972Val
ENST00000642864.1:c.2914C>G MANE Select	ENSP00000495726.1:p.Leu972Val
ENST00000674510.1:c.2914C>G	ENSP00000502054.1:p.Leu972Val
ENST00000674761.1:n.1221C>G
ENST00000675719.1:c.2884C>G	ENSP00000501927.1:p.Leu962Val
ENST00000375365.2:c.2299C>G	ENSP00000364514.2:p.Leu767Val
ENST00000396435.7:c.2914C>G	ENSP00000379712.3:p.Leu972Val
NM_001111125.2:c.2914C>G	NP_001104595.1:p.Leu972Val
NM_015075.1:c.2299C>G	NP_055890.1:p.Leu767Val
XM_006724579.2:c.3010C>G	XP_006724642.1:p.Leu1004Val
XM_006724580.2:c.2299C>G	XP_006724643.1:p.Leu767Val
XM_006724581.2:c.3010C>G	XP_006724644.1:p.Leu1004Val
XM_006724582.2:c.3010C>G	XP_006724645.1:p.Leu1004Val
XM_006724583.2:c.3010C>G	XP_006724646.1:p.Leu1004Val
XM_006724584.2:c.3010C>G	XP_006724647.1:p.Leu1004Val
XM_011530772.1:c.2236C>G	XP_011529074.1:p.Leu746Val
XM_011530773.1:c.2203C>G	XP_011529075.1:p.Leu735Val
XM_011530774.1:c.3010C>G	XP_011529076.1:p.Leu1004Val
XM_011530775.1:c.3010C>G	XP_011529077.1:p.Leu1004Val
XM_011530776.1:c.3010C>G	XP_011529078.1:p.Leu1004Val
XM_011530777.1:c.3010C>G	XP_011529079.1:p.Leu1004Val
XR_938365.1:n.3237C>G
XM_006724579.3:c.3010C>G	XP_006724642.1:p.Leu1004Val
XM_006724580.3:c.2299C>G	XP_006724643.1:p.Leu767Val
XM_006724581.4:c.3010C>G	XP_006724644.1:p.Leu1004Val
XM_006724582.4:c.3010C>G	XP_006724645.1:p.Leu1004Val
XM_006724583.4:c.3010C>G	XP_006724646.1:p.Leu1004Val
XM_006724584.3:c.3010C>G	XP_006724647.1:p.Leu1004Val
XM_011530773.2:c.2203C>G	XP_011529075.1:p.Leu735Val
XM_011530774.3:c.3010C>G	XP_011529076.1:p.Leu1004Val
XM_011530776.2:c.3010C>G	XP_011529078.1:p.Leu1004Val
XM_011530777.2:c.3010C>G	XP_011529079.1:p.Leu1004Val
XM_017029359.2:c.2884C>G	XP_016884848.1:p.Leu962Val
XM_017029360.1:c.2416C>G	XP_016884849.1:p.Leu806Val
XR_938365.2:n.3231C>G
NM_001111125.3:c.2914C>G MANE Select	NP_001104595.1:p.Leu972Val
NM_015075.2:c.2299C>G	NP_055890.1:p.Leu767Val