Canonical Allele Identifier: CA2243993517

Gene: CTNS

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3647582_3647583delinsGC , CM000679.2:g.3647582_3647583delinsGC	GRCh38
NC_000017.10:g.3550876_3550877delinsGC , CM000679.1:g.3550876_3550877delinsGC	GRCh37
NC_000017.9:g.3497625_3497626delinsGC	NCBI36
NG_012489.1:g.16115_16116delinsGC
NG_012489.2:g.16115_16116delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000046640.9:c.140+60_140+61delinsGC MANE Select	ENSP00000046640.4:n.140+60_140+61delinsGC
ENST00000381870.8:c.140+60_140+61delinsGC	ENSP00000371294.3:n.140+60_140+61delinsGC
ENST00000399306.7:c.140+60_140+61delinsGC	ENSP00000382245.2:n.140+60_140+61delinsGC
ENST00000488623.6:c.-588+60_-588+61delinsGC	ENSP00000501016.1:n.-588+60_-588+61delinsGC
ENST00000574776.6:c.-113+7315_-113+7316delinsGC	ENSP00000461118.2:n.-113+7315_-113+7316delinsGC
ENST00000673669.1:c.-217+60_-217+61delinsGC	ENSP00000501123.1:n.-217+60_-217+61delinsGC
ENST00000673965.1:c.140+60_140+61delinsGC	ENSP00000500995.1:n.140+60_140+61delinsGC
ENST00000046640.7:c.140+60_140+61delinsGC	ENSP00000046640.3:n.140+60_140+61delinsGC
ENST00000381870.7:c.140+60_140+61delinsGC	ENSP00000371294.3:n.140+60_140+61delinsGC
ENST00000399306.6:c.140+60_140+61delinsGC	ENSP00000382245.2:n.140+60_140+61delinsGC
ENST00000452111.5:c.140+60_140+61delinsGC	ENSP00000408652.1:n.140+60_140+61delinsGC
ENST00000467663.5:c.140+60_140+61delinsGC	ENSP00000461056.1:n.140+60_140+61delinsGC
ENST00000488623.5:n.361+60_361+61delinsGC
ENST00000495445.5:n.514_515delinsGC
ENST00000574218.1:c.-216-7416_-216-7415delinsGC	ENSP00000458912.1:n.-216-7416_-216-7415delinsGC
ENST00000574776.5:c.-113+7315_-113+7316delinsGC	ENSP00000461118.1:n.-113+7315_-113+7316delinsGC
ENST00000576979.1:c.140+60_140+61delinsGC	ENSP00000458457.1:n.140+60_140+61delinsGC
NM_001031681.2:c.140+60_140+61delinsGC	NP_001026851.2:n.140+60_140+61delinsGC
NM_004937.2:c.140+60_140+61delinsGC	NP_004928.2:n.140+60_140+61delinsGC
XM_005256485.1:c.140+60_140+61delinsGC	XP_005256542.1:n.140+60_140+61delinsGC
XM_006721463.1:c.140+60_140+61delinsGC	XP_006721526.1:n.140+60_140+61delinsGC
XM_006721464.1:c.-217+60_-217+61delinsGC	XP_006721527.1:n.-217+60_-217+61delinsGC
XM_011523691.1:c.140+60_140+61delinsGC	XP_011521993.1:n.140+60_140+61delinsGC
XM_011523692.1:c.-302+60_-302+61delinsGC	XP_011521994.1:n.-302+60_-302+61delinsGC
XR_934003.1:n.733+60_733+61delinsGC
XR_934164.1:n.431-2408_431-2407delinsGC
XM_005256485.3:c.140+60_140+61delinsGC	XP_005256542.1:n.140+60_140+61delinsGC
XM_006721463.3:c.140+60_140+61delinsGC	XP_006721526.1:n.140+60_140+61delinsGC
XM_006721464.2:c.-217+60_-217+61delinsGC	XP_006721527.1:n.-217+60_-217+61delinsGC
XM_011523691.2:c.140+60_140+61delinsGC	XP_011521993.1:n.140+60_140+61delinsGC
XM_011523692.2:c.-302+60_-302+61delinsGC	XP_011521994.1:n.-302+60_-302+61delinsGC
XM_017024254.1:c.-217+7315_-217+7316delinsGC	XP_016879743.1:n.-217+7315_-217+7316delinsGC
XM_017024255.1:c.-217+60_-217+61delinsGC	XP_016879744.1:n.-217+60_-217+61delinsGC
XM_017024256.1:c.-302+60_-302+61delinsGC	XP_016879745.1:n.-302+60_-302+61delinsGC
XM_017024257.1:c.-217+7315_-217+7316delinsGC	XP_016879746.1:n.-217+7315_-217+7316delinsGC
XM_017024258.1:c.-217+60_-217+61delinsGC	XP_016879747.1:n.-217+60_-217+61delinsGC
XR_001752758.1:n.453-2408_453-2407delinsGC
XR_001752759.1:n.325-2408_325-2407delinsGC
XR_001752760.1:n.453-2408_453-2407delinsGC
XR_001752761.2:n.452+2581_452+2582delinsGC
XR_002958115.1:n.140-2408_140-2407delinsGC
XR_934164.2:n.453-2408_453-2407delinsGC
NM_001374492.1:c.140+60_140+61delinsGC	NP_001361421.1:n.140+60_140+61delinsGC
NM_001374493.1:c.-217+60_-217+61delinsGC	NP_001361422.1:n.-217+60_-217+61delinsGC
NM_001374494.1:c.-302+60_-302+61delinsGC	NP_001361423.1:n.-302+60_-302+61delinsGC
NM_001374495.1:c.-217+7315_-217+7316delinsGC	NP_001361424.1:n.-217+7315_-217+7316delinsGC
NM_001374496.1:c.-217+60_-217+61delinsGC	NP_001361425.1:n.-217+60_-217+61delinsGC
NM_004937.3:c.140+60_140+61delinsGC MANE Select	NP_004928.2:n.140+60_140+61delinsGC
NM_001031681.3:c.140+60_140+61delinsGC	NP_001026851.2:n.140+60_140+61delinsGC