Canonical Allele Identifier: CA2243969744

Gene: CTNS

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3636712A= , CM000679.2:g.3636712A=	GRCh38
NC_000017.10:g.3540006A= , CM000679.1:g.3540006A=	GRCh37
NC_000017.9:g.3486755A=	NCBI36
NG_012489.1:g.5245A=
NG_052852.1:g.4611T=
NG_012489.2:g.5245A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000381870.8:c.-230+4A=	ENSP00000371294.3:n.-230+4A=
ENST00000673965.1:c.-230+9A=	ENSP00000500995.1:n.-230+9A=
ENST00000046640.7:c.-349A=	ENSP00000046640.3:n.-349A=
ENST00000381870.7:c.-230+4A=	ENSP00000371294.3:n.-230+4A=
NM_001031681.2:c.-230+4A=	NP_001026851.2:n.-230+4A=
NM_004937.2:c.-349A=	NP_004928.2:n.-349A=
XM_005256485.1:c.-349A=	XP_005256542.1:n.-349A=
XM_006721463.1:c.-230+9A=	XP_006721526.1:n.-230+9A=
XM_006721464.1:c.-705A=	XP_006721527.1:n.-705A=
XM_011523692.1:c.-710A=	XP_011521994.1:n.-710A=
XR_934003.1:n.245A=
XM_005256485.3:c.-349A=	XP_005256542.1:n.-349A=
XM_006721463.3:c.-230+9A=	XP_006721526.1:n.-230+9A=
XM_006721464.2:c.-705A=	XP_006721527.1:n.-705A=
XM_011523692.2:c.-710A=	XP_011521994.1:n.-710A=
XM_017024254.1:c.-626A=	XP_016879743.1:n.-626A=
XM_017024255.1:c.-705A=	XP_016879744.1:n.-705A=
XM_017024256.1:c.-710A=	XP_016879745.1:n.-710A=
XM_017024257.1:c.-626A=	XP_016879746.1:n.-626A=
XM_017024258.1:c.-625A=	XP_016879747.1:n.-625A=
NM_001031681.3:c.-230+4A=	NP_001026851.2:n.-230+4A=