Canonical Allele Identifier: CA980870571
Gene: CTNS HGNC NCBI
CTNS-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2076153461

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3656603_3656610dup , CM000679.2:g.3656603_3656610dup GRCh38
NC_000017.10:g.3559897_3559904dup , CM000679.1:g.3559897_3559904dup GRCh37
NC_000017.9:g.3506646_3506653dup NCBI36
NG_012489.1:g.25136_25143dup
NG_012489.2:g.25136_25143dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000046640.9:c.561+17_561+24dup (CTNS) MANE Select ENSP00000046640.4:n.561+17_561+24dup
ENST00000381870.8:c.561+17_561+24dup (CTNS) ENSP00000371294.3:n.561+17_561+24dup
ENST00000488623.6:c.-193+17_-193+24dup (CTNS) ENSP00000501016.1:n.-193+17_-193+24dup
ENST00000574776.6:c.120+17_120+24dup (CTNS) ENSP00000461118.2:n.120+17_120+24dup
ENST00000673669.1:c.120+17_120+24dup (CTNS) ENSP00000501123.1:n.120+17_120+24dup
ENST00000673965.1:c.561+17_561+24dup (CTNS) ENSP00000500995.1:n.561+17_561+24dup
ENST00000046640.7:c.561+17_561+24dup (CTNS) ENSP00000046640.3:n.561+17_561+24dup
ENST00000381870.7:c.561+17_561+24dup (CTNS) ENSP00000371294.3:n.561+17_561+24dup
NM_001031681.2:c.561+17_561+24dup (CTNS) NP_001026851.2:n.561+17_561+24dup
NM_004937.2:c.561+17_561+24dup (CTNS) NP_004928.2:n.561+17_561+24dup
XM_005256485.1:c.561+17_561+24dup (CTNS) XP_005256542.1:n.561+17_561+24dup
XM_006721463.1:c.561+17_561+24dup (CTNS) XP_006721526.1:n.561+17_561+24dup
XM_006721464.1:c.120+17_120+24dup (CTNS) XP_006721527.1:n.120+17_120+24dup
XM_011523691.1:c.561+17_561+24dup (CTNS) XP_011521993.1:n.561+17_561+24dup
XM_011523692.1:c.120+17_120+24dup (CTNS) XP_011521994.1:n.120+17_120+24dup
XR_934003.1:n.1154+17_1154+24dup (CTNS)
XR_934158.1:n.1143+247_1143+254dup (CTNS-AS1)
XR_934159.1:n.433+247_433+254dup (CTNS-AS1)
XR_934160.1:n.438+247_438+254dup (CTNS-AS1)
XR_934161.1:n.433+247_433+254dup (CTNS-AS1)
XR_934162.1:n.438+247_438+254dup (CTNS-AS1)
XR_934163.1:n.1034+247_1034+254dup (CTNS-AS1)
XM_005256485.3:c.561+17_561+24dup (CTNS) XP_005256542.1:n.561+17_561+24dup
XM_006721463.3:c.561+17_561+24dup (CTNS) XP_006721526.1:n.561+17_561+24dup
XM_006721464.2:c.120+17_120+24dup (CTNS) XP_006721527.1:n.120+17_120+24dup
XM_011523691.2:c.561+17_561+24dup (CTNS) XP_011521993.1:n.561+17_561+24dup
XM_011523692.2:c.120+17_120+24dup (CTNS) XP_011521994.1:n.120+17_120+24dup
XM_017024254.1:c.120+17_120+24dup (CTNS) XP_016879743.1:n.120+17_120+24dup
XM_017024255.1:c.120+17_120+24dup (CTNS) XP_016879744.1:n.120+17_120+24dup
XM_017024256.1:c.120+17_120+24dup (CTNS) XP_016879745.1:n.120+17_120+24dup
XM_017024257.1:c.120+17_120+24dup (CTNS) XP_016879746.1:n.120+17_120+24dup
XM_017024258.1:c.120+17_120+24dup (CTNS) XP_016879747.1:n.120+17_120+24dup
XR_934158.2:n.1160+247_1160+254dup (CTNS-AS1)
XR_934159.2:n.450+247_450+254dup (CTNS-AS1)
XR_934160.2:n.455+247_455+254dup (CTNS-AS1)
XR_934161.2:n.450+247_450+254dup (CTNS-AS1)
XR_934162.3:n.455+247_455+254dup (CTNS-AS1)
XR_934163.2:n.1051+247_1051+254dup (CTNS-AS1)
NM_001374492.1:c.561+17_561+24dup (CTNS) NP_001361421.1:n.561+17_561+24dup
NM_001374493.1:c.120+17_120+24dup (CTNS) NP_001361422.1:n.120+17_120+24dup
NM_001374494.1:c.120+17_120+24dup (CTNS) NP_001361423.1:n.120+17_120+24dup
NM_001374495.1:c.120+17_120+24dup (CTNS) NP_001361424.1:n.120+17_120+24dup
NM_001374496.1:c.120+17_120+24dup (CTNS) NP_001361425.1:n.120+17_120+24dup
NM_004937.3:c.561+17_561+24dup (CTNS) MANE Select NP_004928.2:n.561+17_561+24dup
NM_001031681.3:c.561+17_561+24dup (CTNS) NP_001026851.2:n.561+17_561+24dup