Canonical Allele Identifier: CA2243969677
Gene: CTNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3636607C= , CM000679.2:g.3636607C= GRCh38
NC_000017.10:g.3539901C= , CM000679.1:g.3539901C= GRCh37
NC_000017.9:g.3486650C= NCBI36
NG_012489.1:g.5140C=
NG_052852.1:g.4716G=
NG_012489.2:g.5140C=

Transcript Alleles

HGVS Amino-acid change
ENST00000381870.8:c.-331C= ENSP00000371294.3:n.-331C=
ENST00000673965.1:c.-326C= ENSP00000500995.1:n.-326C=
ENST00000046640.7:c.-454C= ENSP00000046640.3:n.-454C=
ENST00000381870.7:c.-331C= ENSP00000371294.3:n.-331C=
NM_001031681.2:c.-331C= NP_001026851.2:n.-331C=
NM_004937.2:c.-454C= NP_004928.2:n.-454C=
XM_005256485.1:c.-454C= XP_005256542.1:n.-454C=
XM_006721463.1:c.-326C= XP_006721526.1:n.-326C=
XM_006721464.1:c.-810C= XP_006721527.1:n.-810C=
XM_011523692.1:c.-815C= XP_011521994.1:n.-815C=
XR_934003.1:n.140C=
XM_005256485.3:c.-454C= XP_005256542.1:n.-454C=
XM_006721463.3:c.-326C= XP_006721526.1:n.-326C=
XM_006721464.2:c.-810C= XP_006721527.1:n.-810C=
XM_011523692.2:c.-815C= XP_011521994.1:n.-815C=
XM_017024254.1:c.-731C= XP_016879743.1:n.-731C=
XM_017024255.1:c.-810C= XP_016879744.1:n.-810C=
XM_017024256.1:c.-815C= XP_016879745.1:n.-815C=
XM_017024257.1:c.-731C= XP_016879746.1:n.-731C=
XM_017024258.1:c.-730C= XP_016879747.1:n.-730C=
NM_001031681.3:c.-331C= NP_001026851.2:n.-331C=