Canonical Allele Identifier: CA1947825163

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753665C= , CM000673.2:g.1753665C=	GRCh38
NC_000011.9:g.1774895C= , CM000673.1:g.1774895C=	GRCh37
NC_000011.8:g.1731471C=	NCBI36
NG_008655.1:g.15328G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1077G= MANE Select	ENSP00000236671.2:p.Ser359=
ENST00000367196.4:c.972G=	ENSP00000356164.4:p.Ser324=
ENST00000427721.3:c.502G=
ENST00000429746.2:c.972G=	ENSP00000402586.2:p.Ser324=
ENST00000433655.6:c.*243G=	ENSP00000404902.1:n.*243G=
ENST00000438213.6:c.1194G=	ENSP00000415036.2:p.Ser398=
ENST00000497544.3:n.785G=
ENST00000636397.1:c.1071+138G=	ENSP00000489910.1:n.1071+138G=
ENST00000636571.1:c.1056G=	ENSP00000490770.1:p.Ser352=
ENST00000636579.1:c.72+138G=	ENSP00000490489.1:n.72+138G=
ENST00000636615.1:c.1071+138G=	ENSP00000490014.1:n.1071+138G=
ENST00000636843.1:c.1071G=	ENSP00000490897.1:p.Ser357=
ENST00000637158.1:n.675G=
ENST00000637381.2:n.3505G=
ENST00000637387.1:c.1056G=	ENSP00000490598.1:p.Ser352=
ENST00000637815.2:c.1059G=	ENSP00000490344.1:p.Ser353=
ENST00000637915.1:c.1072-4G=	ENSP00000490471.1:n.1072-4G=
ENST00000637937.1:n.385G=
ENST00000678991.1:c.*938G=	ENSP00000503019.1:n.*938G=
ENST00000236671.6:c.1077G=	ENSP00000236671.2:p.Ser359=
ENST00000427721.2:c.471+138G=	ENSP00000415840.2:n.471+138G=
ENST00000429746.1:c.408G=	ENSP00000402586.1:p.Ser136=
ENST00000433655.5:c.*243G=	ENSP00000404902.1:n.*243G=
NM_001909.4:c.1077G=	NP_001900.1:p.Ser359=
NM_001909.5:c.1077G= MANE Select	NP_001900.1:p.Ser359=