Canonical Allele Identifier: CA2635424645
Gene: CTNS HGNC NCBI

Linked Data

gnomAD v4: 17-3660370-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3660370C>T , CM000679.2:g.3660370C>T GRCh38
NC_000017.10:g.3563664C>T , CM000679.1:g.3563664C>T GRCh37
NC_000017.9:g.3510413C>T NCBI36
NG_012489.1:g.28903C>T
NG_012489.2:g.28903C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000046640.9:c.*1C>T MANE Select ENSP00000046640.4:n.*1C>T
ENST00000381870.8:c.1085+20C>T ENSP00000371294.3:n.1085+20C>T
ENST00000488623.6:c.*1C>T ENSP00000501016.1:n.*1C>T
ENST00000574776.6:c.644+20C>T ENSP00000461118.2:n.644+20C>T
ENST00000673669.1:c.*1C>T ENSP00000501123.1:n.*1C>T
ENST00000673965.1:c.*1C>T ENSP00000500995.1:n.*1C>T
ENST00000046640.7:c.*1C>T ENSP00000046640.3:n.*1C>T
ENST00000381870.7:c.1085+20C>T ENSP00000371294.3:n.1085+20C>T
NM_001031681.2:c.1085+20C>T NP_001026851.2:n.1085+20C>T
NM_004937.2:c.*1C>T NP_004928.2:n.*1C>T
XM_005256485.1:c.1085+20C>T XP_005256542.1:n.1085+20C>T
XM_006721463.1:c.1085+20C>T XP_006721526.1:n.1085+20C>T
XM_006721464.1:c.644+20C>T XP_006721527.1:n.644+20C>T
XM_011523691.1:c.1085+20C>T XP_011521993.1:n.1085+20C>T
XM_011523692.1:c.644+20C>T XP_011521994.1:n.644+20C>T
XM_005256485.3:c.1085+20C>T XP_005256542.1:n.1085+20C>T
XM_006721463.3:c.1085+20C>T XP_006721526.1:n.1085+20C>T
XM_006721464.2:c.644+20C>T XP_006721527.1:n.644+20C>T
XM_011523691.2:c.1085+20C>T XP_011521993.1:n.1085+20C>T
XM_011523692.2:c.644+20C>T XP_011521994.1:n.644+20C>T
XM_017024254.1:c.644+20C>T XP_016879743.1:n.644+20C>T
XM_017024255.1:c.*1C>T XP_016879744.1:n.*1C>T
XM_017024256.1:c.*1C>T XP_016879745.1:n.*1C>T
XM_017024257.1:c.*1C>T XP_016879746.1:n.*1C>T
XM_017024258.1:c.*1C>T XP_016879747.1:n.*1C>T
NM_001374492.1:c.1085+20C>T NP_001361421.1:n.1085+20C>T
NM_001374493.1:c.*1C>T NP_001361422.1:n.*1C>T
NM_001374494.1:c.*1C>T NP_001361423.1:n.*1C>T
NM_001374495.1:c.*1C>T NP_001361424.1:n.*1C>T
NM_001374496.1:c.*1C>T NP_001361425.1:n.*1C>T
NM_004937.3:c.*1C>T MANE Select NP_004928.2:n.*1C>T
NM_001031681.3:c.1085+20C>T NP_001026851.2:n.1085+20C>T