Canonical Allele Identifier: CA2576123930

Gene: CTNS

Linked Data

• ClinVar Variation Id: 2925454
• ClinVar RCV Id: RCV003781108

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3659990_3659996del , CM000679.2:g.3659990_3659996del	GRCh38
NC_000017.10:g.3563284_3563290del , CM000679.1:g.3563284_3563290del	GRCh37
NC_000017.9:g.3510033_3510039del	NCBI36
NG_012489.1:g.28523_28529del
NG_012489.2:g.28523_28529del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000046640.9:c.970+15_970+21del MANE Select	ENSP00000046640.4:n.970+15_970+21del
ENST00000381870.8:c.970+15_970+21del	ENSP00000371294.3:n.970+15_970+21del
ENST00000488623.6:c.217+15_217+21del	ENSP00000501016.1:n.217+15_217+21del
ENST00000574776.6:c.529+15_529+21del	ENSP00000461118.2:n.529+15_529+21del
ENST00000673669.1:c.529+15_529+21del	ENSP00000501123.1:n.529+15_529+21del
ENST00000673965.1:c.970+15_970+21del	ENSP00000500995.1:n.970+15_970+21del
ENST00000046640.7:c.970+15_970+21del	ENSP00000046640.3:n.970+15_970+21del
ENST00000381870.7:c.970+15_970+21del	ENSP00000371294.3:n.970+15_970+21del
NM_001031681.2:c.970+15_970+21del	NP_001026851.2:n.970+15_970+21del
NM_004937.2:c.970+15_970+21del	NP_004928.2:n.970+15_970+21del
XM_005256485.1:c.970+15_970+21del	XP_005256542.1:n.970+15_970+21del
XM_006721463.1:c.970+15_970+21del	XP_006721526.1:n.970+15_970+21del
XM_006721464.1:c.529+15_529+21del	XP_006721527.1:n.529+15_529+21del
XM_011523691.1:c.970+15_970+21del	XP_011521993.1:n.970+15_970+21del
XM_011523692.1:c.529+15_529+21del	XP_011521994.1:n.529+15_529+21del
XM_005256485.3:c.970+15_970+21del	XP_005256542.1:n.970+15_970+21del
XM_006721463.3:c.970+15_970+21del	XP_006721526.1:n.970+15_970+21del
XM_006721464.2:c.529+15_529+21del	XP_006721527.1:n.529+15_529+21del
XM_011523691.2:c.970+15_970+21del	XP_011521993.1:n.970+15_970+21del
XM_011523692.2:c.529+15_529+21del	XP_011521994.1:n.529+15_529+21del
XM_017024254.1:c.529+15_529+21del	XP_016879743.1:n.529+15_529+21del
XM_017024255.1:c.529+15_529+21del	XP_016879744.1:n.529+15_529+21del
XM_017024256.1:c.529+15_529+21del	XP_016879745.1:n.529+15_529+21del
XM_017024257.1:c.529+15_529+21del	XP_016879746.1:n.529+15_529+21del
XM_017024258.1:c.529+15_529+21del	XP_016879747.1:n.529+15_529+21del
NM_001374492.1:c.970+15_970+21del	NP_001361421.1:n.970+15_970+21del
NM_001374493.1:c.529+15_529+21del	NP_001361422.1:n.529+15_529+21del
NM_001374494.1:c.529+15_529+21del	NP_001361423.1:n.529+15_529+21del
NM_001374495.1:c.529+15_529+21del	NP_001361424.1:n.529+15_529+21del
NM_001374496.1:c.529+15_529+21del	NP_001361425.1:n.529+15_529+21del
NM_004937.3:c.970+15_970+21del MANE Select	NP_004928.2:n.970+15_970+21del
NM_001031681.3:c.970+15_970+21del	NP_001026851.2:n.970+15_970+21del