Canonical Allele Identifier: CA2243969753
Gene: CTNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3636719A= , CM000679.2:g.3636719A= GRCh38
NC_000017.10:g.3540013A= , CM000679.1:g.3540013A= GRCh37
NC_000017.9:g.3486762A= NCBI36
NG_012489.1:g.5252A=
NG_052852.1:g.4604T=
NG_012489.2:g.5252A=

Transcript Alleles

HGVS Amino-acid change
ENST00000381870.8:c.-230+11A= ENSP00000371294.3:n.-230+11A=
ENST00000673965.1:c.-230+16A= ENSP00000500995.1:n.-230+16A=
ENST00000046640.7:c.-342A= ENSP00000046640.3:n.-342A=
ENST00000381870.7:c.-230+11A= ENSP00000371294.3:n.-230+11A=
NM_001031681.2:c.-230+11A= NP_001026851.2:n.-230+11A=
NM_004937.2:c.-342A= NP_004928.2:n.-342A=
XM_005256485.1:c.-342A= XP_005256542.1:n.-342A=
XM_006721463.1:c.-230+16A= XP_006721526.1:n.-230+16A=
XM_006721464.1:c.-698A= XP_006721527.1:n.-698A=
XM_011523692.1:c.-703A= XP_011521994.1:n.-703A=
XR_934003.1:n.252A=
XM_005256485.3:c.-342A= XP_005256542.1:n.-342A=
XM_006721463.3:c.-230+16A= XP_006721526.1:n.-230+16A=
XM_006721464.2:c.-698A= XP_006721527.1:n.-698A=
XM_011523692.2:c.-703A= XP_011521994.1:n.-703A=
XM_017024254.1:c.-619A= XP_016879743.1:n.-619A=
XM_017024255.1:c.-698A= XP_016879744.1:n.-698A=
XM_017024256.1:c.-703A= XP_016879745.1:n.-703A=
XM_017024257.1:c.-619A= XP_016879746.1:n.-619A=
XM_017024258.1:c.-618A= XP_016879747.1:n.-618A=
NM_001031681.3:c.-230+11A= NP_001026851.2:n.-230+11A=