Canonical Allele Identifier: CA379097223

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1758983G>A , CM000673.2:g.1758983G>A	GRCh38
NC_000011.9:g.1780213G>A , CM000673.1:g.1780213G>A	GRCh37
NC_000011.8:g.1736789G>A	NCBI36
NG_008655.1:g.10010C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001909.5:c.457C>T MANE Select	NP_001900.1:p.Gln153Ter
ENST00000236671.7:c.457C>T MANE Select	ENSP00000236671.2:p.Gln153Ter
NM_001909.4:c.457C>T	NP_001900.1:p.Gln153Ter
ENST00000236671.6:c.457C>T	ENSP00000236671.2:p.Gln153Ter
ENST00000367196.3:c.352C>T	ENSP00000356164.3:p.Gln118Ter
ENST00000367196.4:c.352C>T	ENSP00000356164.4:p.Gln118Ter
ENST00000427721.2:c.-144C>T	ENSP00000415840.2:n.-144C>T
ENST00000429746.2:c.352C>T	ENSP00000402586.2:p.Gln118Ter
ENST00000433655.5:c.457C>T	ENSP00000404902.1:p.Gln153Ter
ENST00000433655.6:c.457C>T	ENSP00000404902.1:p.Gln153Ter
ENST00000438213.5:c.412C>T	ENSP00000415036.1:p.Gln138Ter
ENST00000438213.6:c.457C>T	ENSP00000415036.2:p.Gln153Ter
ENST00000636397.1:c.457C>T	ENSP00000489910.1:p.Gln153Ter
ENST00000636571.1:c.436C>T	ENSP00000490770.1:p.Gln146Ter
ENST00000636615.1:c.457C>T	ENSP00000490014.1:p.Gln153Ter
ENST00000636843.1:c.451C>T	ENSP00000490897.1:p.Gln151Ter
ENST00000637381.2:n.2885C>T
ENST00000637387.1:c.457C>T	ENSP00000490598.1:p.Gln153Ter
ENST00000637815.2:c.457C>T	ENSP00000490344.1:p.Gln153Ter
ENST00000637915.1:c.457C>T	ENSP00000490471.1:p.Gln153Ter
ENST00000677300.1:n.852C>T
ENST00000678991.1:c.*318C>T	ENSP00000503019.1:n.*318C>T