Canonical Allele Identifier: CA1947827596

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1757397C= , CM000673.2:g.1757397C=	GRCh38
NC_000011.9:g.1778627C= , CM000673.1:g.1778627C=	GRCh37
NC_000011.8:g.1735203C=	NCBI36
NG_008655.1:g.11596G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000236671.7:c.631G= MANE Select	ENSP00000236671.2:p.Val211=
ENST00000367196.4:c.526G=	ENSP00000356164.4:p.Val176=
ENST00000427721.3:c.56G=
ENST00000429746.2:c.526G=	ENSP00000402586.2:p.Val176=
ENST00000433655.6:c.631G=	ENSP00000404902.1:p.Val211=
ENST00000438213.6:c.631G=	ENSP00000415036.2:p.Val211=
ENST00000636397.1:c.631G=	ENSP00000489910.1:p.Val211=
ENST00000636571.1:c.610G=	ENSP00000490770.1:p.Val204=
ENST00000636615.1:c.631G=	ENSP00000490014.1:p.Val211=
ENST00000636843.1:c.625G=	ENSP00000490897.1:p.Val209=
ENST00000637158.1:n.229G=
ENST00000637381.2:n.3059G=
ENST00000637387.1:c.631G=	ENSP00000490598.1:p.Val211=
ENST00000637815.2:c.631G=	ENSP00000490344.1:p.Val211=
ENST00000637915.1:c.631G=	ENSP00000490471.1:p.Val211=
ENST00000677300.1:n.1026G=
ENST00000678991.1:c.*492G=	ENSP00000503019.1:n.*492G=
ENST00000236671.6:c.631G=	ENSP00000236671.2:p.Val211=
ENST00000367196.3:c.526G=	ENSP00000356164.3:p.Val176=
ENST00000427721.2:c.31G=	ENSP00000415840.2:p.Val11=
ENST00000433655.5:c.631G=	ENSP00000404902.1:p.Val211=
ENST00000438213.5:c.586G=	ENSP00000415036.1:p.Val196=
NM_001909.4:c.631G=	NP_001900.1:p.Val211=
NM_001909.5:c.631G= MANE Select	NP_001900.1:p.Val211=