Canonical Allele Identifier: CA2243993167
Gene: CTNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3647236G= , CM000679.2:g.3647236G= GRCh38
NC_000017.10:g.3550530G= , CM000679.1:g.3550530G= GRCh37
NC_000017.9:g.3497279G= NCBI36
NG_012489.1:g.15769G=
NG_012489.2:g.15769G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000046640.9:c.62-208G= MANE Select ENSP00000046640.4:n.62-208G=
ENST00000381870.8:c.62-208G= ENSP00000371294.3:n.62-208G=
ENST00000399306.7:c.62-208G= ENSP00000382245.2:n.62-208G=
ENST00000488623.6:c.-666-208G= ENSP00000501016.1:n.-666-208G=
ENST00000574776.6:c.-113+6969G= ENSP00000461118.2:n.-113+6969G=
ENST00000673669.1:c.-295-208G= ENSP00000501123.1:n.-295-208G=
ENST00000673965.1:c.62-208G= ENSP00000500995.1:n.62-208G=
ENST00000046640.7:c.62-208G= ENSP00000046640.3:n.62-208G=
ENST00000381870.7:c.62-208G= ENSP00000371294.3:n.62-208G=
ENST00000399306.6:c.62-208G= ENSP00000382245.2:n.62-208G=
ENST00000452111.5:c.62-208G= ENSP00000408652.1:n.62-208G=
ENST00000467663.5:c.62-208G= ENSP00000461056.1:n.62-208G=
ENST00000488623.5:n.283-208G=
ENST00000495445.5:n.376-208G=
ENST00000574218.1:c.-216-7762G= ENSP00000458912.1:n.-216-7762G=
ENST00000574776.5:c.-113+6969G= ENSP00000461118.1:n.-113+6969G=
ENST00000576979.1:c.62-208G= ENSP00000458457.1:n.62-208G=
NM_001031681.2:c.62-208G= NP_001026851.2:n.62-208G=
NM_004937.2:c.62-208G= NP_004928.2:n.62-208G=
XM_005256485.1:c.62-208G= XP_005256542.1:n.62-208G=
XM_006721463.1:c.62-208G= XP_006721526.1:n.62-208G=
XM_006721464.1:c.-295-208G= XP_006721527.1:n.-295-208G=
XM_011523691.1:c.62-208G= XP_011521993.1:n.62-208G=
XM_011523692.1:c.-380-208G= XP_011521994.1:n.-380-208G=
XR_934003.1:n.655-208G=
XR_934164.1:n.431-2061C=
XM_005256485.3:c.62-208G= XP_005256542.1:n.62-208G=
XM_006721463.3:c.62-208G= XP_006721526.1:n.62-208G=
XM_006721464.2:c.-295-208G= XP_006721527.1:n.-295-208G=
XM_011523691.2:c.62-208G= XP_011521993.1:n.62-208G=
XM_011523692.2:c.-380-208G= XP_011521994.1:n.-380-208G=
XM_017024254.1:c.-217+6969G= XP_016879743.1:n.-217+6969G=
XM_017024255.1:c.-295-208G= XP_016879744.1:n.-295-208G=
XM_017024256.1:c.-380-208G= XP_016879745.1:n.-380-208G=
XM_017024257.1:c.-217+6969G= XP_016879746.1:n.-217+6969G=
XM_017024258.1:c.-295-208G= XP_016879747.1:n.-295-208G=
XR_001752758.1:n.453-2061C=
XR_001752759.1:n.325-2061C=
XR_001752760.1:n.453-2061C=
XR_001752761.2:n.452+2928C=
XR_002958115.1:n.140-2061C=
XR_934164.2:n.453-2061C=
NM_001374492.1:c.62-208G= NP_001361421.1:n.62-208G=
NM_001374493.1:c.-295-208G= NP_001361422.1:n.-295-208G=
NM_001374494.1:c.-380-208G= NP_001361423.1:n.-380-208G=
NM_001374495.1:c.-217+6969G= NP_001361424.1:n.-217+6969G=
NM_001374496.1:c.-295-208G= NP_001361425.1:n.-295-208G=
NM_004937.3:c.62-208G= MANE Select NP_004928.2:n.62-208G=
NM_001031681.3:c.62-208G= NP_001026851.2:n.62-208G=