Canonical Allele Identifier: CA8292005
Gene: CTNS HGNC NCBI

Linked Data

dbSNP Id: rs761185996
gnomAD v2: 17-3563555-C-G
gnomAD v4: 17-3660261-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.3660261C>G , CM000679.2:g.3660261C>G GRCh38
NC_000017.10:g.3563555C>G , CM000679.1:g.3563555C>G GRCh37
NC_000017.9:g.3510304C>G NCBI36
NG_012489.1:g.28794C>G
NG_012489.2:g.28794C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000046640.9:c.996C>G MANE Select ENSP00000046640.4:p.Asp332Glu
ENST00000381870.8:c.996C>G ENSP00000371294.3:p.Asp332Glu
ENST00000488623.6:c.243C>G ENSP00000501016.1:p.Asp81Glu
ENST00000574776.6:c.555C>G ENSP00000461118.2:p.Asp185Glu
ENST00000673669.1:c.555C>G ENSP00000501123.1:p.Asp185Glu
ENST00000673965.1:c.996C>G ENSP00000500995.1:p.Asp332Glu
ENST00000046640.7:c.996C>G ENSP00000046640.3:p.Asp332Glu
ENST00000381870.7:c.996C>G ENSP00000371294.3:p.Asp332Glu
NM_001031681.2:c.996C>G NP_001026851.2:p.Asp332Glu
NM_004937.2:c.996C>G NP_004928.2:p.Asp332Glu
XM_005256485.1:c.996C>G XP_005256542.1:p.Asp332Glu
XM_006721463.1:c.996C>G XP_006721526.1:p.Asp332Glu
XM_006721464.1:c.555C>G XP_006721527.1:p.Asp185Glu
XM_011523691.1:c.996C>G XP_011521993.1:p.Asp332Glu
XM_011523692.1:c.555C>G XP_011521994.1:p.Asp185Glu
XM_005256485.3:c.996C>G XP_005256542.1:p.Asp332Glu
XM_006721463.3:c.996C>G XP_006721526.1:p.Asp332Glu
XM_006721464.2:c.555C>G XP_006721527.1:p.Asp185Glu
XM_011523691.2:c.996C>G XP_011521993.1:p.Asp332Glu
XM_011523692.2:c.555C>G XP_011521994.1:p.Asp185Glu
XM_017024254.1:c.555C>G XP_016879743.1:p.Asp185Glu
XM_017024255.1:c.555C>G XP_016879744.1:p.Asp185Glu
XM_017024256.1:c.555C>G XP_016879745.1:p.Asp185Glu
XM_017024257.1:c.555C>G XP_016879746.1:p.Asp185Glu
XM_017024258.1:c.555C>G XP_016879747.1:p.Asp185Glu
NM_001374492.1:c.996C>G NP_001361421.1:p.Asp332Glu
NM_001374493.1:c.555C>G NP_001361422.1:p.Asp185Glu
NM_001374494.1:c.555C>G NP_001361423.1:p.Asp185Glu
NM_001374495.1:c.555C>G NP_001361424.1:p.Asp185Glu
NM_001374496.1:c.555C>G NP_001361425.1:p.Asp185Glu
NM_004937.3:c.996C>G MANE Select NP_004928.2:p.Asp332Glu
NM_001031681.3:c.996C>G NP_001026851.2:p.Asp332Glu