Canonical Allele Identifier: CA2243978478

Gene: CTNS

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.3659865T= , CM000679.2:g.3659865T=	GRCh38
NC_000017.10:g.3563159T= , CM000679.1:g.3563159T=	GRCh37
NC_000017.9:g.3509908T=	NCBI36
NG_012489.1:g.28398T=
NG_012489.2:g.28398T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000046640.9:c.860T= MANE Select	ENSP00000046640.4:p.Met287=
ENST00000381870.8:c.860T=	ENSP00000371294.3:p.Met287=
ENST00000488623.6:c.107T=	ENSP00000501016.1:p.Met36=
ENST00000574776.6:c.419T=	ENSP00000461118.2:p.Met140=
ENST00000673669.1:c.419T=	ENSP00000501123.1:p.Met140=
ENST00000673965.1:c.860T=	ENSP00000500995.1:p.Met287=
ENST00000046640.7:c.860T=	ENSP00000046640.3:p.Met287=
ENST00000381870.7:c.860T=	ENSP00000371294.3:p.Met287=
NM_001031681.2:c.860T=	NP_001026851.2:p.Met287=
NM_004937.2:c.860T=	NP_004928.2:p.Met287=
XM_005256485.1:c.860T=	XP_005256542.1:p.Met287=
XM_006721463.1:c.860T=	XP_006721526.1:p.Met287=
XM_006721464.1:c.419T=	XP_006721527.1:p.Met140=
XM_011523691.1:c.860T=	XP_011521993.1:p.Met287=
XM_011523692.1:c.419T=	XP_011521994.1:p.Met140=
XR_934003.1:n.2786T=
XM_005256485.3:c.860T=	XP_005256542.1:p.Met287=
XM_006721463.3:c.860T=	XP_006721526.1:p.Met287=
XM_006721464.2:c.419T=	XP_006721527.1:p.Met140=
XM_011523691.2:c.860T=	XP_011521993.1:p.Met287=
XM_011523692.2:c.419T=	XP_011521994.1:p.Met140=
XM_017024254.1:c.419T=	XP_016879743.1:p.Met140=
XM_017024255.1:c.419T=	XP_016879744.1:p.Met140=
XM_017024256.1:c.419T=	XP_016879745.1:p.Met140=
XM_017024257.1:c.419T=	XP_016879746.1:p.Met140=
XM_017024258.1:c.419T=	XP_016879747.1:p.Met140=
NM_001374492.1:c.860T=	NP_001361421.1:p.Met287=
NM_001374493.1:c.419T=	NP_001361422.1:p.Met140=
NM_001374494.1:c.419T=	NP_001361423.1:p.Met140=
NM_001374495.1:c.419T=	NP_001361424.1:p.Met140=
NM_001374496.1:c.419T=	NP_001361425.1:p.Met140=
NM_004937.3:c.860T= MANE Select	NP_004928.2:p.Met287=
NM_001031681.3:c.860T=	NP_001026851.2:p.Met287=