Canonical Allele Identifier: CA2243969756
Gene: CTNS HGNC NCBI

Linked Data

dbSNP Id: rs2075537513
gnomAD v3: 17-3636722-C-A
gnomAD v4: 17-3636722-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3636722C>A , CM000679.2:g.3636722C>A GRCh38
NC_000017.10:g.3540016C>A , CM000679.1:g.3540016C>A GRCh37
NC_000017.9:g.3486765C>A NCBI36
NG_012489.1:g.5255C>A
NG_052852.1:g.4601G>T
NG_012489.2:g.5255C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000381870.8:c.-230+14C>A ENSP00000371294.3:n.-230+14C>A
ENST00000673965.1:c.-230+19C>A ENSP00000500995.1:n.-230+19C>A
ENST00000046640.7:c.-339C>A ENSP00000046640.3:n.-339C>A
ENST00000381870.7:c.-230+14C>A ENSP00000371294.3:n.-230+14C>A
NM_001031681.2:c.-230+14C>A NP_001026851.2:n.-230+14C>A
NM_004937.2:c.-339C>A NP_004928.2:n.-339C>A
XM_005256485.1:c.-339C>A XP_005256542.1:n.-339C>A
XM_006721463.1:c.-230+19C>A XP_006721526.1:n.-230+19C>A
XM_006721464.1:c.-695C>A XP_006721527.1:n.-695C>A
XM_011523692.1:c.-700C>A XP_011521994.1:n.-700C>A
XR_934003.1:n.255C>A
XM_005256485.3:c.-339C>A XP_005256542.1:n.-339C>A
XM_006721463.3:c.-230+19C>A XP_006721526.1:n.-230+19C>A
XM_006721464.2:c.-695C>A XP_006721527.1:n.-695C>A
XM_011523692.2:c.-700C>A XP_011521994.1:n.-700C>A
XM_017024254.1:c.-616C>A XP_016879743.1:n.-616C>A
XM_017024255.1:c.-695C>A XP_016879744.1:n.-695C>A
XM_017024256.1:c.-700C>A XP_016879745.1:n.-700C>A
XM_017024257.1:c.-616C>A XP_016879746.1:n.-616C>A
XM_017024258.1:c.-615C>A XP_016879747.1:n.-615C>A
NM_001031681.3:c.-230+14C>A NP_001026851.2:n.-230+14C>A