Canonical Allele Identifier: CA2243969675
Gene: CTNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3636603C= , CM000679.2:g.3636603C= GRCh38
NC_000017.10:g.3539897C= , CM000679.1:g.3539897C= GRCh37
NC_000017.9:g.3486646C= NCBI36
NG_012489.1:g.5136C=
NG_052852.1:g.4720G=
NG_012489.2:g.5136C=

Transcript Alleles

HGVS Amino-acid change
ENST00000381870.8:c.-335C= ENSP00000371294.3:n.-335C=
ENST00000673965.1:c.-330C= ENSP00000500995.1:n.-330C=
ENST00000046640.7:c.-458C= ENSP00000046640.3:n.-458C=
ENST00000381870.7:c.-335C= ENSP00000371294.3:n.-335C=
NM_001031681.2:c.-335C= NP_001026851.2:n.-335C=
NM_004937.2:c.-458C= NP_004928.2:n.-458C=
XM_005256485.1:c.-458C= XP_005256542.1:n.-458C=
XM_006721463.1:c.-330C= XP_006721526.1:n.-330C=
XM_006721464.1:c.-814C= XP_006721527.1:n.-814C=
XM_011523692.1:c.-819C= XP_011521994.1:n.-819C=
XR_934003.1:n.136C=
XM_005256485.3:c.-458C= XP_005256542.1:n.-458C=
XM_006721463.3:c.-330C= XP_006721526.1:n.-330C=
XM_006721464.2:c.-814C= XP_006721527.1:n.-814C=
XM_011523692.2:c.-819C= XP_011521994.1:n.-819C=
XM_017024254.1:c.-735C= XP_016879743.1:n.-735C=
XM_017024255.1:c.-814C= XP_016879744.1:n.-814C=
XM_017024256.1:c.-819C= XP_016879745.1:n.-819C=
XM_017024257.1:c.-735C= XP_016879746.1:n.-735C=
XM_017024258.1:c.-734C= XP_016879747.1:n.-734C=
NM_001031681.3:c.-335C= NP_001026851.2:n.-335C=