Canonical Allele Identifier: CA2243969599

Gene: CTNS

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3636504C= , CM000679.2:g.3636504C=	GRCh38
NC_000017.10:g.3539798C= , CM000679.1:g.3539798C=	GRCh37
NC_000017.9:g.3486547C=	NCBI36
NG_012489.1:g.5037C=
NG_052852.1:g.4819G=
NG_012489.2:g.5037C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381870.8:c.-434C=	ENSP00000371294.3:n.-434C=
ENST00000673965.1:c.-429C=	ENSP00000500995.1:n.-429C=
ENST00000046640.7:c.-557C=	ENSP00000046640.3:n.-557C=
ENST00000381870.7:c.-434C=	ENSP00000371294.3:n.-434C=
NM_001031681.2:c.-434C=	NP_001026851.2:n.-434C=
NM_004937.2:c.-557C=	NP_004928.2:n.-557C=
XM_005256485.1:c.-557C=	XP_005256542.1:n.-557C=
XM_006721463.1:c.-429C=	XP_006721526.1:n.-429C=
XM_006721464.1:c.-913C=	XP_006721527.1:n.-913C=
XM_011523692.1:c.-918C=	XP_011521994.1:n.-918C=
XR_934003.1:n.37C=
XM_005256485.3:c.-557C=	XP_005256542.1:n.-557C=
XM_006721463.3:c.-429C=	XP_006721526.1:n.-429C=
XM_006721464.2:c.-913C=	XP_006721527.1:n.-913C=
XM_011523692.2:c.-918C=	XP_011521994.1:n.-918C=
XM_017024254.1:c.-834C=	XP_016879743.1:n.-834C=
XM_017024255.1:c.-913C=	XP_016879744.1:n.-913C=
XM_017024256.1:c.-918C=	XP_016879745.1:n.-918C=
XM_017024257.1:c.-834C=	XP_016879746.1:n.-834C=
XM_017024258.1:c.-833C=	XP_016879747.1:n.-833C=
NM_001031681.3:c.-434C=	NP_001026851.2:n.-434C=