Canonical Allele Identifier: CA2243969743

Gene: CTNS

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3636708G= , CM000679.2:g.3636708G=	GRCh38
NC_000017.10:g.3540002G= , CM000679.1:g.3540002G=	GRCh37
NC_000017.9:g.3486751G=	NCBI36
NG_012489.1:g.5241G=
NG_052852.1:g.4615C=
NG_012489.2:g.5241G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381870.8:c.-230G=	ENSP00000371294.3:n.-230G=
ENST00000673965.1:c.-230+5G=	ENSP00000500995.1:n.-230+5G=
ENST00000046640.7:c.-353G=	ENSP00000046640.3:n.-353G=
ENST00000381870.7:c.-230G=	ENSP00000371294.3:n.-230G=
NM_001031681.2:c.-230G=	NP_001026851.2:n.-230G=
NM_004937.2:c.-353G=	NP_004928.2:n.-353G=
XM_005256485.1:c.-353G=	XP_005256542.1:n.-353G=
XM_006721463.1:c.-230+5G=	XP_006721526.1:n.-230+5G=
XM_006721464.1:c.-709G=	XP_006721527.1:n.-709G=
XM_011523692.1:c.-714G=	XP_011521994.1:n.-714G=
XR_934003.1:n.241G=
XM_005256485.3:c.-353G=	XP_005256542.1:n.-353G=
XM_006721463.3:c.-230+5G=	XP_006721526.1:n.-230+5G=
XM_006721464.2:c.-709G=	XP_006721527.1:n.-709G=
XM_011523692.2:c.-714G=	XP_011521994.1:n.-714G=
XM_017024254.1:c.-630G=	XP_016879743.1:n.-630G=
XM_017024255.1:c.-709G=	XP_016879744.1:n.-709G=
XM_017024256.1:c.-714G=	XP_016879745.1:n.-714G=
XM_017024257.1:c.-630G=	XP_016879746.1:n.-630G=
XM_017024258.1:c.-629G=	XP_016879747.1:n.-629G=
NM_001031681.3:c.-230G=	NP_001026851.2:n.-230G=