Canonical Allele Identifier: CA728484120

Gene: CTNS CTNS-AS1

Linked Data

• dbSNP Id: rs1400859720
• gnomAD v4: 17-3654901-G-A
• MyVariant Identifiers: chr17:g.3558195G>A (hg19) ; chr17:g.3654901G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3654901G>A , CM000679.2:g.3654901G>A	GRCh38
NC_000017.10:g.3558195G>A , CM000679.1:g.3558195G>A	GRCh37
NC_000017.9:g.3504944G>A	NCBI36
NG_012489.1:g.23434G>A
NG_012489.2:g.23434G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000046640.9:c.226-97G>A (CTNS) MANE Select	ENSP00000046640.4:n.226-97G>A
ENST00000381870.8:c.226-97G>A (CTNS)	ENSP00000371294.3:n.226-97G>A
ENST00000488623.6:c.-502-97G>A (CTNS)	ENSP00000501016.1:n.-502-97G>A
ENST00000574776.6:c.-112-320G>A (CTNS)	ENSP00000461118.2:n.-112-320G>A
ENST00000673669.1:c.-216-97G>A (CTNS)	ENSP00000501123.1:n.-216-97G>A
ENST00000673965.1:c.226-97G>A (CTNS)	ENSP00000500995.1:n.226-97G>A
ENST00000046640.7:c.226-97G>A (CTNS)	ENSP00000046640.3:n.226-97G>A
ENST00000381870.7:c.226-97G>A (CTNS)	ENSP00000371294.3:n.226-97G>A
ENST00000467663.5:c.141-97G>A (CTNS)	ENSP00000461056.1:n.141-97G>A
ENST00000488623.5:n.447-97G>A (CTNS)
ENST00000574218.1:c.-216-97G>A (CTNS)	ENSP00000458912.1:n.-216-97G>A
ENST00000574776.5:c.-112-320G>A (CTNS)	ENSP00000461118.1:n.-112-320G>A
ENST00000576979.1:c.226-97G>A (CTNS)	ENSP00000458457.1:n.226-97G>A
NM_001031681.2:c.226-97G>A (CTNS)	NP_001026851.2:n.226-97G>A
NM_004937.2:c.226-97G>A (CTNS)	NP_004928.2:n.226-97G>A
XM_005256485.1:c.226-97G>A (CTNS)	XP_005256542.1:n.226-97G>A
XM_006721463.1:c.226-97G>A (CTNS)	XP_006721526.1:n.226-97G>A
XM_006721464.1:c.-216-97G>A (CTNS)	XP_006721527.1:n.-216-97G>A
XM_011523691.1:c.226-97G>A (CTNS)	XP_011521993.1:n.226-97G>A
XM_011523692.1:c.-216-97G>A (CTNS)	XP_011521994.1:n.-216-97G>A
XR_934003.1:n.819-97G>A (CTNS)
XR_934158.1:n.1143+1955C>T (CTNS-AS1)
XR_934159.1:n.433+1955C>T (CTNS-AS1)
XR_934160.1:n.438+1955C>T (CTNS-AS1)
XR_934163.1:n.1034+1955C>T (CTNS-AS1)
XM_005256485.3:c.226-97G>A (CTNS)	XP_005256542.1:n.226-97G>A
XM_006721463.3:c.226-97G>A (CTNS)	XP_006721526.1:n.226-97G>A
XM_006721464.2:c.-216-97G>A (CTNS)	XP_006721527.1:n.-216-97G>A
XM_011523691.2:c.226-97G>A (CTNS)	XP_011521993.1:n.226-97G>A
XM_011523692.2:c.-216-97G>A (CTNS)	XP_011521994.1:n.-216-97G>A
XM_017024254.1:c.-216-97G>A (CTNS)	XP_016879743.1:n.-216-97G>A
XM_017024255.1:c.-216-97G>A (CTNS)	XP_016879744.1:n.-216-97G>A
XM_017024256.1:c.-216-97G>A (CTNS)	XP_016879745.1:n.-216-97G>A
XM_017024257.1:c.-216-97G>A (CTNS)	XP_016879746.1:n.-216-97G>A
XM_017024258.1:c.-216-97G>A (CTNS)	XP_016879747.1:n.-216-97G>A
XR_934158.2:n.1160+1955C>T (CTNS-AS1)
XR_934159.2:n.450+1955C>T (CTNS-AS1)
XR_934160.2:n.455+1955C>T (CTNS-AS1)
XR_934163.2:n.1051+1955C>T (CTNS-AS1)
NM_001374492.1:c.226-97G>A (CTNS)	NP_001361421.1:n.226-97G>A
NM_001374493.1:c.-216-97G>A (CTNS)	NP_001361422.1:n.-216-97G>A
NM_001374494.1:c.-216-97G>A (CTNS)	NP_001361423.1:n.-216-97G>A
NM_001374495.1:c.-216-97G>A (CTNS)	NP_001361424.1:n.-216-97G>A
NM_001374496.1:c.-216-97G>A (CTNS)	NP_001361425.1:n.-216-97G>A
NM_004937.3:c.226-97G>A (CTNS) MANE Select	NP_004928.2:n.226-97G>A
NM_001031681.3:c.226-97G>A (CTNS)	NP_001026851.2:n.226-97G>A