Canonical Allele Identifier: CA2243969736
Gene: CTNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3636697G= , CM000679.2:g.3636697G= GRCh38
NC_000017.10:g.3539991G= , CM000679.1:g.3539991G= GRCh37
NC_000017.9:g.3486740G= NCBI36
NG_012489.1:g.5230G=
NG_052852.1:g.4626C=
NG_012489.2:g.5230G=

Transcript Alleles

HGVS Amino-acid change
ENST00000381870.8:c.-241G= ENSP00000371294.3:n.-241G=
ENST00000673965.1:c.-236G= ENSP00000500995.1:n.-236G=
ENST00000046640.7:c.-364G= ENSP00000046640.3:n.-364G=
ENST00000381870.7:c.-241G= ENSP00000371294.3:n.-241G=
NM_001031681.2:c.-241G= NP_001026851.2:n.-241G=
NM_004937.2:c.-364G= NP_004928.2:n.-364G=
XM_005256485.1:c.-364G= XP_005256542.1:n.-364G=
XM_006721463.1:c.-236G= XP_006721526.1:n.-236G=
XM_006721464.1:c.-720G= XP_006721527.1:n.-720G=
XM_011523692.1:c.-725G= XP_011521994.1:n.-725G=
XR_934003.1:n.230G=
XM_005256485.3:c.-364G= XP_005256542.1:n.-364G=
XM_006721463.3:c.-236G= XP_006721526.1:n.-236G=
XM_006721464.2:c.-720G= XP_006721527.1:n.-720G=
XM_011523692.2:c.-725G= XP_011521994.1:n.-725G=
XM_017024254.1:c.-641G= XP_016879743.1:n.-641G=
XM_017024255.1:c.-720G= XP_016879744.1:n.-720G=
XM_017024256.1:c.-725G= XP_016879745.1:n.-725G=
XM_017024257.1:c.-641G= XP_016879746.1:n.-641G=
XM_017024258.1:c.-640G= XP_016879747.1:n.-640G=
NM_001031681.3:c.-241G= NP_001026851.2:n.-241G=