Canonical Allele Identifier: CA397687895

Gene: CTNS

Linked Data

• MyVariant Identifiers: chr17:g.3552169A>G (hg19) ; chr17:g.3648875A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3648875A>G , CM000679.2:g.3648875A>G	GRCh38
NC_000017.10:g.3552169A>G , CM000679.1:g.3552169A>G	GRCh37
NC_000017.9:g.3498918A>G	NCBI36
NG_012489.1:g.17408A>G
NG_012489.2:g.17408A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000046640.9:c.169A>G MANE Select	ENSP00000046640.4:p.Thr57Ala
ENST00000381870.8:c.169A>G	ENSP00000371294.3:p.Thr57Ala
ENST00000399306.7:c.169A>G	ENSP00000382245.2:p.Thr57Ala
ENST00000488623.6:c.-559A>G	ENSP00000501016.1:n.-559A>G
ENST00000574776.6:c.-112-6346A>G	ENSP00000461118.2:n.-112-6346A>G
ENST00000673669.1:c.-217+1353A>G	ENSP00000501123.1:n.-217+1353A>G
ENST00000673965.1:c.169A>G	ENSP00000500995.1:p.Thr57Ala
ENST00000046640.7:c.169A>G	ENSP00000046640.3:p.Thr57Ala
ENST00000381870.7:c.169A>G	ENSP00000371294.3:p.Thr57Ala
ENST00000399306.6:c.169A>G	ENSP00000382245.2:p.Thr57Ala
ENST00000452111.5:c.169A>G	ENSP00000408652.1:p.Thr57Ala
ENST00000467663.5:c.140+1353A>G	ENSP00000461056.1:n.140+1353A>G
ENST00000488623.5:n.390A>G
ENST00000574218.1:c.-216-6123A>G	ENSP00000458912.1:n.-216-6123A>G
ENST00000574776.5:c.-112-6346A>G	ENSP00000461118.1:n.-112-6346A>G
ENST00000576979.1:c.169A>G	ENSP00000458457.1:p.Thr57Ala
NM_001031681.2:c.169A>G	NP_001026851.2:p.Thr57Ala
NM_004937.2:c.169A>G	NP_004928.2:p.Thr57Ala
XM_005256485.1:c.169A>G	XP_005256542.1:p.Thr57Ala
XM_006721463.1:c.169A>G	XP_006721526.1:p.Thr57Ala
XM_006721464.1:c.-217+1353A>G	XP_006721527.1:n.-217+1353A>G
XM_011523691.1:c.169A>G	XP_011521993.1:p.Thr57Ala
XM_011523692.1:c.-273A>G	XP_011521994.1:n.-273A>G
XR_934003.1:n.762A>G
XR_934164.1:n.430+1289T>C
XM_005256485.3:c.169A>G	XP_005256542.1:p.Thr57Ala
XM_006721463.3:c.169A>G	XP_006721526.1:p.Thr57Ala
XM_006721464.2:c.-217+1353A>G	XP_006721527.1:n.-217+1353A>G
XM_011523691.2:c.169A>G	XP_011521993.1:p.Thr57Ala
XM_011523692.2:c.-273A>G	XP_011521994.1:n.-273A>G
XM_017024254.1:c.-216-6123A>G	XP_016879743.1:n.-216-6123A>G
XM_017024255.1:c.-217+1353A>G	XP_016879744.1:n.-217+1353A>G
XM_017024256.1:c.-273A>G	XP_016879745.1:n.-273A>G
XM_017024257.1:c.-216-6123A>G	XP_016879746.1:n.-216-6123A>G
XM_017024258.1:c.-217+1353A>G	XP_016879747.1:n.-217+1353A>G
XR_001752758.1:n.452+1289T>C
XR_001752759.1:n.324+1289T>C
XR_001752760.1:n.452+1289T>C
XR_001752761.2:n.452+1289T>C
XR_002958115.1:n.139+1289T>C
XR_934164.2:n.452+1289T>C
NM_001374492.1:c.169A>G	NP_001361421.1:p.Thr57Ala
NM_001374493.1:c.-217+1353A>G	NP_001361422.1:n.-217+1353A>G
NM_001374494.1:c.-273A>G	NP_001361423.1:n.-273A>G
NM_001374495.1:c.-216-6123A>G	NP_001361424.1:n.-216-6123A>G
NM_001374496.1:c.-217+1353A>G	NP_001361425.1:n.-217+1353A>G
NM_004937.3:c.169A>G MANE Select	NP_004928.2:p.Thr57Ala
NM_001031681.3:c.169A>G	NP_001026851.2:p.Thr57Ala