Canonical Allele Identifier: CA2243969693

Gene: CTNS

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3636628C= , CM000679.2:g.3636628C=	GRCh38
NC_000017.10:g.3539922C= , CM000679.1:g.3539922C=	GRCh37
NC_000017.9:g.3486671C=	NCBI36
NG_012489.1:g.5161C=
NG_052852.1:g.4695G=
NG_012489.2:g.5161C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381870.8:c.-310C=	ENSP00000371294.3:n.-310C=
ENST00000673965.1:c.-305C=	ENSP00000500995.1:n.-305C=
ENST00000046640.7:c.-433C=	ENSP00000046640.3:n.-433C=
ENST00000381870.7:c.-310C=	ENSP00000371294.3:n.-310C=
NM_001031681.2:c.-310C=	NP_001026851.2:n.-310C=
NM_004937.2:c.-433C=	NP_004928.2:n.-433C=
XM_005256485.1:c.-433C=	XP_005256542.1:n.-433C=
XM_006721463.1:c.-305C=	XP_006721526.1:n.-305C=
XM_006721464.1:c.-789C=	XP_006721527.1:n.-789C=
XM_011523692.1:c.-794C=	XP_011521994.1:n.-794C=
XR_934003.1:n.161C=
XM_005256485.3:c.-433C=	XP_005256542.1:n.-433C=
XM_006721463.3:c.-305C=	XP_006721526.1:n.-305C=
XM_006721464.2:c.-789C=	XP_006721527.1:n.-789C=
XM_011523692.2:c.-794C=	XP_011521994.1:n.-794C=
XM_017024254.1:c.-710C=	XP_016879743.1:n.-710C=
XM_017024255.1:c.-789C=	XP_016879744.1:n.-789C=
XM_017024256.1:c.-794C=	XP_016879745.1:n.-794C=
XM_017024257.1:c.-710C=	XP_016879746.1:n.-710C=
XM_017024258.1:c.-709C=	XP_016879747.1:n.-709C=
NM_001031681.3:c.-310C=	NP_001026851.2:n.-310C=