Canonical Allele Identifier: CA1947825376

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1754003A= , CM000673.2:g.1754003A=	GRCh38
NC_000011.9:g.1775233A= , CM000673.1:g.1775233A=	GRCh37
NC_000011.8:g.1731809A=	NCBI36
NG_008655.1:g.14990T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.963T= MANE Select	ENSP00000236671.2:p.Ile321=
ENST00000367196.4:c.858T=	ENSP00000356164.4:p.Ile286=
ENST00000427721.3:c.388T=
ENST00000429746.2:c.858T=	ENSP00000402586.2:p.Ile286=
ENST00000433655.6:c.*129T=	ENSP00000404902.1:n.*129T=
ENST00000438213.6:c.1080T=	ENSP00000415036.2:p.Ile360=
ENST00000497544.3:n.579T=
ENST00000636397.1:c.963T=	ENSP00000489910.1:p.Ile321=
ENST00000636571.1:c.942T=	ENSP00000490770.1:p.Ile314=
ENST00000636615.1:c.963T=	ENSP00000490014.1:p.Ile321=
ENST00000636843.1:c.957T=	ENSP00000490897.1:p.Ile319=
ENST00000637158.1:n.561T=
ENST00000637381.2:n.3391T=
ENST00000637387.1:c.963T=	ENSP00000490598.1:p.Ile321=
ENST00000637815.2:c.945T=	ENSP00000490344.1:p.Ile315=
ENST00000637915.1:c.963T=	ENSP00000490471.1:p.Ile321=
ENST00000637937.1:n.271T=
ENST00000678991.1:c.*824T=	ENSP00000503019.1:n.*824T=
ENST00000236671.6:c.963T=	ENSP00000236671.2:p.Ile321=
ENST00000427721.2:c.363T=	ENSP00000415840.2:p.Ile121=
ENST00000429746.1:c.294T=	ENSP00000402586.1:p.Ile98=
ENST00000433655.5:c.*129T=	ENSP00000404902.1:n.*129T=
ENST00000497544.1:n.579T=
NM_001909.4:c.963T=	NP_001900.1:p.Ile321=
NM_001909.5:c.963T= MANE Select	NP_001900.1:p.Ile321=