Canonical Allele Identifier: CA2513702813

Gene: CTNS

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3647265dup , CM000679.2:g.3647265dup	GRCh38
NC_000017.10:g.3550559dup , CM000679.1:g.3550559dup	GRCh37
NC_000017.9:g.3497308dup	NCBI36
NG_012489.1:g.15798dup
NG_012489.2:g.15798dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000046640.9:c.62-179dup MANE Select	ENSP00000046640.4:n.62-179dup
ENST00000381870.8:c.62-179dup	ENSP00000371294.3:n.62-179dup
ENST00000399306.7:c.62-179dup	ENSP00000382245.2:n.62-179dup
ENST00000488623.6:c.-666-179dup	ENSP00000501016.1:n.-666-179dup
ENST00000574776.6:c.-113+6998dup	ENSP00000461118.2:n.-113+6998dup
ENST00000673669.1:c.-295-179dup	ENSP00000501123.1:n.-295-179dup
ENST00000673965.1:c.62-179dup	ENSP00000500995.1:n.62-179dup
ENST00000046640.7:c.62-179dup	ENSP00000046640.3:n.62-179dup
ENST00000381870.7:c.62-179dup	ENSP00000371294.3:n.62-179dup
ENST00000399306.6:c.62-179dup	ENSP00000382245.2:n.62-179dup
ENST00000452111.5:c.62-179dup	ENSP00000408652.1:n.62-179dup
ENST00000467663.5:c.62-179dup	ENSP00000461056.1:n.62-179dup
ENST00000488623.5:n.283-179dup
ENST00000495445.5:n.376-179dup
ENST00000574218.1:c.-216-7733dup	ENSP00000458912.1:n.-216-7733dup
ENST00000574776.5:c.-113+6998dup	ENSP00000461118.1:n.-113+6998dup
ENST00000576979.1:c.62-179dup	ENSP00000458457.1:n.62-179dup
NM_001031681.2:c.62-179dup	NP_001026851.2:n.62-179dup
NM_004937.2:c.62-179dup	NP_004928.2:n.62-179dup
XM_005256485.1:c.62-179dup	XP_005256542.1:n.62-179dup
XM_006721463.1:c.62-179dup	XP_006721526.1:n.62-179dup
XM_006721464.1:c.-295-179dup	XP_006721527.1:n.-295-179dup
XM_011523691.1:c.62-179dup	XP_011521993.1:n.62-179dup
XM_011523692.1:c.-380-179dup	XP_011521994.1:n.-380-179dup
XR_934003.1:n.655-179dup
XR_934164.1:n.431-2090dup
XM_005256485.3:c.62-179dup	XP_005256542.1:n.62-179dup
XM_006721463.3:c.62-179dup	XP_006721526.1:n.62-179dup
XM_006721464.2:c.-295-179dup	XP_006721527.1:n.-295-179dup
XM_011523691.2:c.62-179dup	XP_011521993.1:n.62-179dup
XM_011523692.2:c.-380-179dup	XP_011521994.1:n.-380-179dup
XM_017024254.1:c.-217+6998dup	XP_016879743.1:n.-217+6998dup
XM_017024255.1:c.-295-179dup	XP_016879744.1:n.-295-179dup
XM_017024256.1:c.-380-179dup	XP_016879745.1:n.-380-179dup
XM_017024257.1:c.-217+6998dup	XP_016879746.1:n.-217+6998dup
XM_017024258.1:c.-295-179dup	XP_016879747.1:n.-295-179dup
XR_001752758.1:n.453-2090dup
XR_001752759.1:n.325-2090dup
XR_001752760.1:n.453-2090dup
XR_001752761.2:n.452+2899dup
XR_002958115.1:n.140-2090dup
XR_934164.2:n.453-2090dup
NM_001374492.1:c.62-179dup	NP_001361421.1:n.62-179dup
NM_001374493.1:c.-295-179dup	NP_001361422.1:n.-295-179dup
NM_001374494.1:c.-380-179dup	NP_001361423.1:n.-380-179dup
NM_001374495.1:c.-217+6998dup	NP_001361424.1:n.-217+6998dup
NM_001374496.1:c.-295-179dup	NP_001361425.1:n.-295-179dup
NM_004937.3:c.62-179dup MANE Select	NP_004928.2:n.62-179dup
NM_001031681.3:c.62-179dup	NP_001026851.2:n.62-179dup