Canonical Allele Identifier: CA2243970091
Gene: CTNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3637284G= , CM000679.2:g.3637284G= GRCh38
NC_000017.10:g.3540578G= , CM000679.1:g.3540578G= GRCh37
NC_000017.9:g.3487327G= NCBI36
NG_012489.1:g.5817G=
NG_052852.1:g.4039C=
NG_012489.2:g.5817G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000046640.9:c.-52G= MANE Select ENSP00000046640.4:n.-52G=
ENST00000381870.8:c.-52G= ENSP00000371294.3:n.-52G=
ENST00000399306.7:c.-52G= ENSP00000382245.2:n.-52G=
ENST00000488623.6:c.-699G= ENSP00000501016.1:n.-699G=
ENST00000574776.6:c.-225G= ENSP00000461118.2:n.-225G=
ENST00000673669.1:c.-328G= ENSP00000501123.1:n.-328G=
ENST00000673965.1:c.-52G= ENSP00000500995.1:n.-52G=
ENST00000046640.7:c.-52G= ENSP00000046640.3:n.-52G=
ENST00000381870.7:c.-52G= ENSP00000371294.3:n.-52G=
ENST00000399306.6:c.-52G= ENSP00000382245.2:n.-52G=
ENST00000452111.5:c.-52G= ENSP00000408652.1:n.-52G=
ENST00000467663.5:c.-52G= ENSP00000461056.1:n.-52G=
ENST00000488623.5:n.250G=
ENST00000495445.5:n.263G=
ENST00000574218.1:c.-249G= ENSP00000458912.1:n.-249G=
ENST00000574776.5:c.-225G= ENSP00000461118.1:n.-225G=
NM_001031681.2:c.-52G= NP_001026851.2:n.-52G=
NM_004937.2:c.-52G= NP_004928.2:n.-52G=
XM_005256485.1:c.-52G= XP_005256542.1:n.-52G=
XM_006721463.1:c.-52G= XP_006721526.1:n.-52G=
XM_006721464.1:c.-408G= XP_006721527.1:n.-408G=
XM_011523691.1:c.-52G= XP_011521993.1:n.-52G=
XM_011523692.1:c.-413G= XP_011521994.1:n.-413G=
XR_934003.1:n.542G=
XM_005256485.3:c.-52G= XP_005256542.1:n.-52G=
XM_006721463.3:c.-52G= XP_006721526.1:n.-52G=
XM_006721464.2:c.-408G= XP_006721527.1:n.-408G=
XM_011523691.2:c.-52G= XP_011521993.1:n.-52G=
XM_011523692.2:c.-413G= XP_011521994.1:n.-413G=
XM_017024254.1:c.-329G= XP_016879743.1:n.-329G=
XM_017024255.1:c.-408G= XP_016879744.1:n.-408G=
XM_017024256.1:c.-413G= XP_016879745.1:n.-413G=
XM_017024257.1:c.-329G= XP_016879746.1:n.-329G=
XM_017024258.1:c.-328G= XP_016879747.1:n.-328G=
NM_001374492.1:c.-52G= NP_001361421.1:n.-52G=
NM_001374493.1:c.-408G= NP_001361422.1:n.-408G=
NM_001374494.1:c.-413G= NP_001361423.1:n.-413G=
NM_001374495.1:c.-329G= NP_001361424.1:n.-329G=
NM_001374496.1:c.-328G= NP_001361425.1:n.-328G=
NM_004937.3:c.-52G= MANE Select NP_004928.2:n.-52G=
NM_001031681.3:c.-52G= NP_001026851.2:n.-52G=