Canonical Allele Identifier: CA2243969739
Gene: CTNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3636700G= , CM000679.2:g.3636700G= GRCh38
NC_000017.10:g.3539994G= , CM000679.1:g.3539994G= GRCh37
NC_000017.9:g.3486743G= NCBI36
NG_012489.1:g.5233G=
NG_052852.1:g.4623C=
NG_012489.2:g.5233G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381870.8:c.-238G= ENSP00000371294.3:n.-238G=
ENST00000673965.1:c.-233G= ENSP00000500995.1:n.-233G=
ENST00000046640.7:c.-361G= ENSP00000046640.3:n.-361G=
ENST00000381870.7:c.-238G= ENSP00000371294.3:n.-238G=
NM_001031681.2:c.-238G= NP_001026851.2:n.-238G=
NM_004937.2:c.-361G= NP_004928.2:n.-361G=
XM_005256485.1:c.-361G= XP_005256542.1:n.-361G=
XM_006721463.1:c.-233G= XP_006721526.1:n.-233G=
XM_006721464.1:c.-717G= XP_006721527.1:n.-717G=
XM_011523692.1:c.-722G= XP_011521994.1:n.-722G=
XR_934003.1:n.233G=
XM_005256485.3:c.-361G= XP_005256542.1:n.-361G=
XM_006721463.3:c.-233G= XP_006721526.1:n.-233G=
XM_006721464.2:c.-717G= XP_006721527.1:n.-717G=
XM_011523692.2:c.-722G= XP_011521994.1:n.-722G=
XM_017024254.1:c.-638G= XP_016879743.1:n.-638G=
XM_017024255.1:c.-717G= XP_016879744.1:n.-717G=
XM_017024256.1:c.-722G= XP_016879745.1:n.-722G=
XM_017024257.1:c.-638G= XP_016879746.1:n.-638G=
XM_017024258.1:c.-637G= XP_016879747.1:n.-637G=
NM_001031681.3:c.-238G= NP_001026851.2:n.-238G=