Canonical Allele Identifier: CA2243993380
Gene: CTNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3647498C= , CM000679.2:g.3647498C= GRCh38
NC_000017.10:g.3550792C= , CM000679.1:g.3550792C= GRCh37
NC_000017.9:g.3497541C= NCBI36
NG_012489.1:g.16031C=
NG_012489.2:g.16031C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000046640.9:c.116C= MANE Select ENSP00000046640.4:p.Ser39=
ENST00000381870.8:c.116C= ENSP00000371294.3:p.Ser39=
ENST00000399306.7:c.116C= ENSP00000382245.2:p.Ser39=
ENST00000488623.6:c.-612C= ENSP00000501016.1:n.-612C=
ENST00000574776.6:c.-113+7231C= ENSP00000461118.2:n.-113+7231C=
ENST00000673669.1:c.-241C= ENSP00000501123.1:n.-241C=
ENST00000673965.1:c.116C= ENSP00000500995.1:p.Ser39=
ENST00000046640.7:c.116C= ENSP00000046640.3:p.Ser39=
ENST00000381870.7:c.116C= ENSP00000371294.3:p.Ser39=
ENST00000399306.6:c.116C= ENSP00000382245.2:p.Ser39=
ENST00000452111.5:c.116C= ENSP00000408652.1:p.Ser39=
ENST00000467663.5:c.116C= ENSP00000461056.1:p.Ser39=
ENST00000488623.5:n.337C=
ENST00000495445.5:n.430C=
ENST00000574218.1:c.-216-7500C= ENSP00000458912.1:n.-216-7500C=
ENST00000574776.5:c.-113+7231C= ENSP00000461118.1:n.-113+7231C=
ENST00000576979.1:c.116C= ENSP00000458457.1:p.Ser39=
NM_001031681.2:c.116C= NP_001026851.2:p.Ser39=
NM_004937.2:c.116C= NP_004928.2:p.Ser39=
XM_005256485.1:c.116C= XP_005256542.1:p.Ser39=
XM_006721463.1:c.116C= XP_006721526.1:p.Ser39=
XM_006721464.1:c.-241C= XP_006721527.1:n.-241C=
XM_011523691.1:c.116C= XP_011521993.1:p.Ser39=
XM_011523692.1:c.-326C= XP_011521994.1:n.-326C=
XR_934003.1:n.709C=
XR_934164.1:n.431-2323G=
XM_005256485.3:c.116C= XP_005256542.1:p.Ser39=
XM_006721463.3:c.116C= XP_006721526.1:p.Ser39=
XM_006721464.2:c.-241C= XP_006721527.1:n.-241C=
XM_011523691.2:c.116C= XP_011521993.1:p.Ser39=
XM_011523692.2:c.-326C= XP_011521994.1:n.-326C=
XM_017024254.1:c.-217+7231C= XP_016879743.1:n.-217+7231C=
XM_017024255.1:c.-241C= XP_016879744.1:n.-241C=
XM_017024256.1:c.-326C= XP_016879745.1:n.-326C=
XM_017024257.1:c.-217+7231C= XP_016879746.1:n.-217+7231C=
XM_017024258.1:c.-241C= XP_016879747.1:n.-241C=
XR_001752758.1:n.453-2323G=
XR_001752759.1:n.325-2323G=
XR_001752760.1:n.453-2323G=
XR_001752761.2:n.452+2666G=
XR_002958115.1:n.140-2323G=
XR_934164.2:n.453-2323G=
NM_001374492.1:c.116C= NP_001361421.1:p.Ser39=
NM_001374493.1:c.-241C= NP_001361422.1:n.-241C=
NM_001374494.1:c.-326C= NP_001361423.1:n.-326C=
NM_001374495.1:c.-217+7231C= NP_001361424.1:n.-217+7231C=
NM_001374496.1:c.-241C= NP_001361425.1:n.-241C=
NM_004937.3:c.116C= MANE Select NP_004928.2:p.Ser39=
NM_001031681.3:c.116C= NP_001026851.2:p.Ser39=