Canonical Allele Identifier: CA2243970078

Gene: CTNS

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3637255_3637256delinsTC , CM000679.2:g.3637255_3637256delinsTC	GRCh38
NC_000017.10:g.3540549_3540550delinsTC , CM000679.1:g.3540549_3540550delinsTC	GRCh37
NC_000017.9:g.3487298_3487299delinsTC	NCBI36
NG_012489.1:g.5788_5789delinsTC
NG_052852.1:g.4067_4068delinsGA
NG_012489.2:g.5788_5789delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000046640.9:c.-81_-80delinsTC MANE Select	ENSP00000046640.4:n.-81_-80delinsTC
ENST00000381870.8:c.-81_-80delinsTC	ENSP00000371294.3:n.-81_-80delinsTC
ENST00000399306.7:c.-81_-80delinsTC	ENSP00000382245.2:n.-81_-80delinsTC
ENST00000488623.6:c.-728_-727delinsTC	ENSP00000501016.1:n.-728_-727delinsTC
ENST00000574776.6:c.-254_-253delinsTC	ENSP00000461118.2:n.-254_-253delinsTC
ENST00000673669.1:c.-357_-356delinsTC	ENSP00000501123.1:n.-357_-356delinsTC
ENST00000673965.1:c.-81_-80delinsTC	ENSP00000500995.1:n.-81_-80delinsTC
ENST00000046640.7:c.-81_-80delinsTC	ENSP00000046640.3:n.-81_-80delinsTC
ENST00000381870.7:c.-81_-80delinsTC	ENSP00000371294.3:n.-81_-80delinsTC
ENST00000399306.6:c.-81_-80delinsTC	ENSP00000382245.2:n.-81_-80delinsTC
ENST00000452111.5:c.-81_-80delinsTC	ENSP00000408652.1:n.-81_-80delinsTC
ENST00000467663.5:c.-81_-80delinsTC	ENSP00000461056.1:n.-81_-80delinsTC
ENST00000488623.5:n.221_222delinsTC
ENST00000495445.5:n.234_235delinsTC
ENST00000574218.1:c.-278_-277delinsTC	ENSP00000458912.1:n.-278_-277delinsTC
ENST00000574776.5:c.-254_-253delinsTC	ENSP00000461118.1:n.-254_-253delinsTC
NM_001031681.2:c.-81_-80delinsTC	NP_001026851.2:n.-81_-80delinsTC
NM_004937.2:c.-81_-80delinsTC	NP_004928.2:n.-81_-80delinsTC
XM_005256485.1:c.-81_-80delinsTC	XP_005256542.1:n.-81_-80delinsTC
XM_006721463.1:c.-81_-80delinsTC	XP_006721526.1:n.-81_-80delinsTC
XM_006721464.1:c.-437_-436delinsTC	XP_006721527.1:n.-437_-436delinsTC
XM_011523691.1:c.-81_-80delinsTC	XP_011521993.1:n.-81_-80delinsTC
XM_011523692.1:c.-442_-441delinsTC	XP_011521994.1:n.-442_-441delinsTC
XR_934003.1:n.513_514delinsTC
XM_005256485.3:c.-81_-80delinsTC	XP_005256542.1:n.-81_-80delinsTC
XM_006721463.3:c.-81_-80delinsTC	XP_006721526.1:n.-81_-80delinsTC
XM_006721464.2:c.-437_-436delinsTC	XP_006721527.1:n.-437_-436delinsTC
XM_011523691.2:c.-81_-80delinsTC	XP_011521993.1:n.-81_-80delinsTC
XM_011523692.2:c.-442_-441delinsTC	XP_011521994.1:n.-442_-441delinsTC
XM_017024254.1:c.-358_-357delinsTC	XP_016879743.1:n.-358_-357delinsTC
XM_017024255.1:c.-437_-436delinsTC	XP_016879744.1:n.-437_-436delinsTC
XM_017024256.1:c.-442_-441delinsTC	XP_016879745.1:n.-442_-441delinsTC
XM_017024257.1:c.-358_-357delinsTC	XP_016879746.1:n.-358_-357delinsTC
XM_017024258.1:c.-357_-356delinsTC	XP_016879747.1:n.-357_-356delinsTC
NM_001374492.1:c.-81_-80delinsTC	NP_001361421.1:n.-81_-80delinsTC
NM_001374493.1:c.-437_-436delinsTC	NP_001361422.1:n.-437_-436delinsTC
NM_001374494.1:c.-442_-441delinsTC	NP_001361423.1:n.-442_-441delinsTC
NM_001374495.1:c.-358_-357delinsTC	NP_001361424.1:n.-358_-357delinsTC
NM_001374496.1:c.-357_-356delinsTC	NP_001361425.1:n.-357_-356delinsTC
NM_004937.3:c.-81_-80delinsTC MANE Select	NP_004928.2:n.-81_-80delinsTC
NM_001031681.3:c.-81_-80delinsTC	NP_001026851.2:n.-81_-80delinsTC