Canonical Allele Identifier: CA2243994721

Gene: CTNS

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3649072C= , CM000679.2:g.3649072C=	GRCh38
NC_000017.10:g.3552366C= , CM000679.1:g.3552366C=	GRCh37
NC_000017.9:g.3499115C=	NCBI36
NG_012489.1:g.17605C=
NG_012489.2:g.17605C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000046640.9:c.225+141C= MANE Select	ENSP00000046640.4:n.225+141C=
ENST00000381870.8:c.225+141C=	ENSP00000371294.3:n.225+141C=
ENST00000399306.7:c.225+141C=	ENSP00000382245.2:n.225+141C=
ENST00000488623.6:c.-503+141C=	ENSP00000501016.1:n.-503+141C=
ENST00000574776.6:c.-112-6149C=	ENSP00000461118.2:n.-112-6149C=
ENST00000673669.1:c.-217+1550C=	ENSP00000501123.1:n.-217+1550C=
ENST00000673965.1:c.225+141C=	ENSP00000500995.1:n.225+141C=
ENST00000046640.7:c.225+141C=	ENSP00000046640.3:n.225+141C=
ENST00000381870.7:c.225+141C=	ENSP00000371294.3:n.225+141C=
ENST00000399306.6:c.225+141C=	ENSP00000382245.2:n.225+141C=
ENST00000467663.5:c.140+1550C=	ENSP00000461056.1:n.140+1550C=
ENST00000488623.5:n.446+141C=
ENST00000574218.1:c.-216-5926C=	ENSP00000458912.1:n.-216-5926C=
ENST00000574776.5:c.-112-6149C=	ENSP00000461118.1:n.-112-6149C=
ENST00000576979.1:c.225+141C=	ENSP00000458457.1:n.225+141C=
NM_001031681.2:c.225+141C=	NP_001026851.2:n.225+141C=
NM_004937.2:c.225+141C=	NP_004928.2:n.225+141C=
XM_005256485.1:c.225+141C=	XP_005256542.1:n.225+141C=
XM_006721463.1:c.225+141C=	XP_006721526.1:n.225+141C=
XM_006721464.1:c.-217+1550C=	XP_006721527.1:n.-217+1550C=
XM_011523691.1:c.225+141C=	XP_011521993.1:n.225+141C=
XM_011523692.1:c.-217+141C=	XP_011521994.1:n.-217+141C=
XR_934003.1:n.818+141C=
XR_934164.1:n.430+1092G=
XM_005256485.3:c.225+141C=	XP_005256542.1:n.225+141C=
XM_006721463.3:c.225+141C=	XP_006721526.1:n.225+141C=
XM_006721464.2:c.-217+1550C=	XP_006721527.1:n.-217+1550C=
XM_011523691.2:c.225+141C=	XP_011521993.1:n.225+141C=
XM_011523692.2:c.-217+141C=	XP_011521994.1:n.-217+141C=
XM_017024254.1:c.-216-5926C=	XP_016879743.1:n.-216-5926C=
XM_017024255.1:c.-217+1550C=	XP_016879744.1:n.-217+1550C=
XM_017024256.1:c.-217+141C=	XP_016879745.1:n.-217+141C=
XM_017024257.1:c.-216-5926C=	XP_016879746.1:n.-216-5926C=
XM_017024258.1:c.-217+1550C=	XP_016879747.1:n.-217+1550C=
XR_001752758.1:n.452+1092G=
XR_001752759.1:n.324+1092G=
XR_001752760.1:n.452+1092G=
XR_001752761.2:n.452+1092G=
XR_002958115.1:n.139+1092G=
XR_934164.2:n.452+1092G=
NM_001374492.1:c.225+141C=	NP_001361421.1:n.225+141C=
NM_001374493.1:c.-217+1550C=	NP_001361422.1:n.-217+1550C=
NM_001374494.1:c.-217+141C=	NP_001361423.1:n.-217+141C=
NM_001374495.1:c.-216-5926C=	NP_001361424.1:n.-216-5926C=
NM_001374496.1:c.-217+1550C=	NP_001361425.1:n.-217+1550C=
NM_004937.3:c.225+141C= MANE Select	NP_004928.2:n.225+141C=
NM_001031681.3:c.225+141C=	NP_001026851.2:n.225+141C=