Canonical Allele Identifier: CA497661258

Gene: CTNS CTNS-AS1

Linked Data

• MyVariant Identifiers: chr17:g.3558551C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3655257C>A , CM000679.2:g.3655257C>A	GRCh38
NC_000017.10:g.3558551C>A , CM000679.1:g.3558551C>A	GRCh37
NC_000017.9:g.3505300C>A	NCBI36
NG_012489.1:g.23790C>A
NG_012489.2:g.23790C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000046640.9:c.366C>A (CTNS) MANE Select	ENSP00000046640.4:p.Ala122=
ENST00000381870.8:c.366C>A (CTNS)	ENSP00000371294.3:p.Ala122=
ENST00000488623.6:c.-362C>A (CTNS)	ENSP00000501016.1:n.-362C>A
ENST00000574776.6:c.-76C>A (CTNS)	ENSP00000461118.2:n.-76C>A
ENST00000673669.1:c.-76C>A (CTNS)	ENSP00000501123.1:n.-76C>A
ENST00000673965.1:c.366C>A (CTNS)	ENSP00000500995.1:p.Ala122=
ENST00000046640.7:c.366C>A (CTNS)	ENSP00000046640.3:p.Ala122=
ENST00000381870.7:c.366C>A (CTNS)	ENSP00000371294.3:p.Ala122=
ENST00000467663.5:c.*119C>A (CTNS)	ENSP00000461056.1:n.*119C>A
ENST00000574218.1:c.-76C>A (CTNS)	ENSP00000458912.1:n.-76C>A
ENST00000574776.5:c.-76C>A (CTNS)	ENSP00000461118.1:n.-76C>A
ENST00000576979.1:c.366C>A (CTNS)	ENSP00000458457.1:p.Ala122=
NM_001031681.2:c.366C>A (CTNS)	NP_001026851.2:p.Ala122=
NM_004937.2:c.366C>A (CTNS)	NP_004928.2:p.Ala122=
XM_005256485.1:c.366C>A (CTNS)	XP_005256542.1:p.Ala122=
XM_006721463.1:c.366C>A (CTNS)	XP_006721526.1:p.Ala122=
XM_006721464.1:c.-76C>A (CTNS)	XP_006721527.1:n.-76C>A
XM_011523691.1:c.366C>A (CTNS)	XP_011521993.1:p.Ala122=
XM_011523692.1:c.-76C>A (CTNS)	XP_011521994.1:n.-76C>A
XR_934003.1:n.959C>A (CTNS)
XR_934158.1:n.1143+1599G>T (CTNS-AS1)
XR_934159.1:n.433+1599G>T (CTNS-AS1)
XR_934160.1:n.438+1599G>T (CTNS-AS1)
XR_934163.1:n.1034+1599G>T (CTNS-AS1)
XM_005256485.3:c.366C>A (CTNS)	XP_005256542.1:p.Ala122=
XM_006721463.3:c.366C>A (CTNS)	XP_006721526.1:p.Ala122=
XM_006721464.2:c.-76C>A (CTNS)	XP_006721527.1:n.-76C>A
XM_011523691.2:c.366C>A (CTNS)	XP_011521993.1:p.Ala122=
XM_011523692.2:c.-76C>A (CTNS)	XP_011521994.1:n.-76C>A
XM_017024254.1:c.-76C>A (CTNS)	XP_016879743.1:n.-76C>A
XM_017024255.1:c.-76C>A (CTNS)	XP_016879744.1:n.-76C>A
XM_017024256.1:c.-76C>A (CTNS)	XP_016879745.1:n.-76C>A
XM_017024257.1:c.-76C>A (CTNS)	XP_016879746.1:n.-76C>A
XM_017024258.1:c.-76C>A (CTNS)	XP_016879747.1:n.-76C>A
XR_934158.2:n.1160+1599G>T (CTNS-AS1)
XR_934159.2:n.450+1599G>T (CTNS-AS1)
XR_934160.2:n.455+1599G>T (CTNS-AS1)
XR_934163.2:n.1051+1599G>T (CTNS-AS1)
NM_001374492.1:c.366C>A (CTNS)	NP_001361421.1:p.Ala122=
NM_001374493.1:c.-76C>A (CTNS)	NP_001361422.1:n.-76C>A
NM_001374494.1:c.-76C>A (CTNS)	NP_001361423.1:n.-76C>A
NM_001374495.1:c.-76C>A (CTNS)	NP_001361424.1:n.-76C>A
NM_001374496.1:c.-76C>A (CTNS)	NP_001361425.1:n.-76C>A
NM_004937.3:c.366C>A (CTNS) MANE Select	NP_004928.2:p.Ala122=
NM_001031681.3:c.366C>A (CTNS)	NP_001026851.2:p.Ala122=