Canonical Allele Identifier: CA1947825377

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1754009C= , CM000673.2:g.1754009C=	GRCh38
NC_000011.9:g.1775239C= , CM000673.1:g.1775239C=	GRCh37
NC_000011.8:g.1731815C=	NCBI36
NG_008655.1:g.14984G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.957G= MANE Select	ENSP00000236671.2:p.Pro319=
ENST00000367196.4:c.852G=	ENSP00000356164.4:p.Pro284=
ENST00000427721.3:c.382G=
ENST00000429746.2:c.852G=	ENSP00000402586.2:p.Pro284=
ENST00000433655.6:c.*123G=	ENSP00000404902.1:n.*123G=
ENST00000438213.6:c.1074G=	ENSP00000415036.2:p.Pro358=
ENST00000497544.3:n.573G=
ENST00000636397.1:c.957G=	ENSP00000489910.1:p.Pro319=
ENST00000636571.1:c.936G=	ENSP00000490770.1:p.Pro312=
ENST00000636615.1:c.957G=	ENSP00000490014.1:p.Pro319=
ENST00000636843.1:c.951G=	ENSP00000490897.1:p.Pro317=
ENST00000637158.1:n.555G=
ENST00000637381.2:n.3385G=
ENST00000637387.1:c.957G=	ENSP00000490598.1:p.Pro319=
ENST00000637815.2:c.939G=	ENSP00000490344.1:p.Pro313=
ENST00000637915.1:c.957G=	ENSP00000490471.1:p.Pro319=
ENST00000637937.1:n.265G=
ENST00000678991.1:c.*818G=	ENSP00000503019.1:n.*818G=
ENST00000236671.6:c.957G=	ENSP00000236671.2:p.Pro319=
ENST00000427721.2:c.357G=	ENSP00000415840.2:p.Pro119=
ENST00000429746.1:c.288G=	ENSP00000402586.1:p.Pro96=
ENST00000433655.5:c.*123G=	ENSP00000404902.1:n.*123G=
ENST00000497544.1:n.573G=
NM_001909.4:c.957G=	NP_001900.1:p.Pro319=
NM_001909.5:c.957G= MANE Select	NP_001900.1:p.Pro319=