Canonical Allele Identifier: CA2243970094
Gene: CTNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3637296T= , CM000679.2:g.3637296T= GRCh38
NC_000017.10:g.3540590T= , CM000679.1:g.3540590T= GRCh37
NC_000017.9:g.3487339T= NCBI36
NG_012489.1:g.5829T=
NG_052852.1:g.4027A=
NG_012489.2:g.5829T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000046640.9:c.-40T= MANE Select ENSP00000046640.4:n.-40T=
ENST00000381870.8:c.-40T= ENSP00000371294.3:n.-40T=
ENST00000399306.7:c.-40T= ENSP00000382245.2:n.-40T=
ENST00000488623.6:c.-687T= ENSP00000501016.1:n.-687T=
ENST00000574776.6:c.-213T= ENSP00000461118.2:n.-213T=
ENST00000673669.1:c.-316T= ENSP00000501123.1:n.-316T=
ENST00000673965.1:c.-40T= ENSP00000500995.1:n.-40T=
ENST00000046640.7:c.-40T= ENSP00000046640.3:n.-40T=
ENST00000381870.7:c.-40T= ENSP00000371294.3:n.-40T=
ENST00000399306.6:c.-40T= ENSP00000382245.2:n.-40T=
ENST00000452111.5:c.-40T= ENSP00000408652.1:n.-40T=
ENST00000467663.5:c.-40T= ENSP00000461056.1:n.-40T=
ENST00000488623.5:n.262T=
ENST00000495445.5:n.275T=
ENST00000574218.1:c.-237T= ENSP00000458912.1:n.-237T=
ENST00000574776.5:c.-213T= ENSP00000461118.1:n.-213T=
NM_001031681.2:c.-40T= NP_001026851.2:n.-40T=
NM_004937.2:c.-40T= NP_004928.2:n.-40T=
XM_005256485.1:c.-40T= XP_005256542.1:n.-40T=
XM_006721463.1:c.-40T= XP_006721526.1:n.-40T=
XM_006721464.1:c.-396T= XP_006721527.1:n.-396T=
XM_011523691.1:c.-40T= XP_011521993.1:n.-40T=
XM_011523692.1:c.-401T= XP_011521994.1:n.-401T=
XR_934003.1:n.554T=
XM_005256485.3:c.-40T= XP_005256542.1:n.-40T=
XM_006721463.3:c.-40T= XP_006721526.1:n.-40T=
XM_006721464.2:c.-396T= XP_006721527.1:n.-396T=
XM_011523691.2:c.-40T= XP_011521993.1:n.-40T=
XM_011523692.2:c.-401T= XP_011521994.1:n.-401T=
XM_017024254.1:c.-317T= XP_016879743.1:n.-317T=
XM_017024255.1:c.-396T= XP_016879744.1:n.-396T=
XM_017024256.1:c.-401T= XP_016879745.1:n.-401T=
XM_017024257.1:c.-317T= XP_016879746.1:n.-317T=
XM_017024258.1:c.-316T= XP_016879747.1:n.-316T=
NM_001374492.1:c.-40T= NP_001361421.1:n.-40T=
NM_001374493.1:c.-396T= NP_001361422.1:n.-396T=
NM_001374494.1:c.-401T= NP_001361423.1:n.-401T=
NM_001374495.1:c.-317T= NP_001361424.1:n.-317T=
NM_001374496.1:c.-316T= NP_001361425.1:n.-316T=
NM_004937.3:c.-40T= MANE Select NP_004928.2:n.-40T=
NM_001031681.3:c.-40T= NP_001026851.2:n.-40T=