Canonical Allele Identifier: CA2243969741
Gene: CTNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3636706C= , CM000679.2:g.3636706C= GRCh38
NC_000017.10:g.3540000C= , CM000679.1:g.3540000C= GRCh37
NC_000017.9:g.3486749C= NCBI36
NG_012489.1:g.5239C=
NG_052852.1:g.4617G=
NG_012489.2:g.5239C=

Transcript Alleles

HGVS Amino-acid change
ENST00000381870.8:c.-232C= ENSP00000371294.3:n.-232C=
ENST00000673965.1:c.-230+3C= ENSP00000500995.1:n.-230+3C=
ENST00000046640.7:c.-355C= ENSP00000046640.3:n.-355C=
ENST00000381870.7:c.-232C= ENSP00000371294.3:n.-232C=
NM_001031681.2:c.-232C= NP_001026851.2:n.-232C=
NM_004937.2:c.-355C= NP_004928.2:n.-355C=
XM_005256485.1:c.-355C= XP_005256542.1:n.-355C=
XM_006721463.1:c.-230+3C= XP_006721526.1:n.-230+3C=
XM_006721464.1:c.-711C= XP_006721527.1:n.-711C=
XM_011523692.1:c.-716C= XP_011521994.1:n.-716C=
XR_934003.1:n.239C=
XM_005256485.3:c.-355C= XP_005256542.1:n.-355C=
XM_006721463.3:c.-230+3C= XP_006721526.1:n.-230+3C=
XM_006721464.2:c.-711C= XP_006721527.1:n.-711C=
XM_011523692.2:c.-716C= XP_011521994.1:n.-716C=
XM_017024254.1:c.-632C= XP_016879743.1:n.-632C=
XM_017024255.1:c.-711C= XP_016879744.1:n.-711C=
XM_017024256.1:c.-716C= XP_016879745.1:n.-716C=
XM_017024257.1:c.-632C= XP_016879746.1:n.-632C=
XM_017024258.1:c.-631C= XP_016879747.1:n.-631C=
NM_001031681.3:c.-232C= NP_001026851.2:n.-232C=