Canonical Allele Identifier: CA2243969740
Gene: CTNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3636704G= , CM000679.2:g.3636704G= GRCh38
NC_000017.10:g.3539998G= , CM000679.1:g.3539998G= GRCh37
NC_000017.9:g.3486747G= NCBI36
NG_012489.1:g.5237G=
NG_052852.1:g.4619C=
NG_012489.2:g.5237G=

Transcript Alleles

HGVS Amino-acid change
ENST00000381870.8:c.-234G= ENSP00000371294.3:n.-234G=
ENST00000673965.1:c.-230+1G= ENSP00000500995.1:n.-230+1G=
ENST00000046640.7:c.-357G= ENSP00000046640.3:n.-357G=
ENST00000381870.7:c.-234G= ENSP00000371294.3:n.-234G=
NM_001031681.2:c.-234G= NP_001026851.2:n.-234G=
NM_004937.2:c.-357G= NP_004928.2:n.-357G=
XM_005256485.1:c.-357G= XP_005256542.1:n.-357G=
XM_006721463.1:c.-230+1G= XP_006721526.1:n.-230+1G=
XM_006721464.1:c.-713G= XP_006721527.1:n.-713G=
XM_011523692.1:c.-718G= XP_011521994.1:n.-718G=
XR_934003.1:n.237G=
XM_005256485.3:c.-357G= XP_005256542.1:n.-357G=
XM_006721463.3:c.-230+1G= XP_006721526.1:n.-230+1G=
XM_006721464.2:c.-713G= XP_006721527.1:n.-713G=
XM_011523692.2:c.-718G= XP_011521994.1:n.-718G=
XM_017024254.1:c.-634G= XP_016879743.1:n.-634G=
XM_017024255.1:c.-713G= XP_016879744.1:n.-713G=
XM_017024256.1:c.-718G= XP_016879745.1:n.-718G=
XM_017024257.1:c.-634G= XP_016879746.1:n.-634G=
XM_017024258.1:c.-633G= XP_016879747.1:n.-633G=
NM_001031681.3:c.-234G= NP_001026851.2:n.-234G=