Canonical Allele Identifier: CA472140866

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1774886C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753656C>A , CM000673.2:g.1753656C>A	GRCh38
NC_000011.9:g.1774886C>A , CM000673.1:g.1774886C>A	GRCh37
NC_000011.8:g.1731462C>A	NCBI36
NG_008655.1:g.15337G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1086G>T MANE Select	ENSP00000236671.2:p.Gly362=
ENST00000367196.4:c.981G>T	ENSP00000356164.4:p.Gly327=
ENST00000427721.3:c.511G>T
ENST00000429746.2:c.981G>T	ENSP00000402586.2:p.Gly327=
ENST00000433655.6:c.*252G>T	ENSP00000404902.1:n.*252G>T
ENST00000438213.6:c.1203G>T	ENSP00000415036.2:p.Gly401=
ENST00000497544.3:n.794G>T
ENST00000636397.1:c.1071+147G>T	ENSP00000489910.1:n.1071+147G>T
ENST00000636571.1:c.1065G>T	ENSP00000490770.1:p.Gly355=
ENST00000636579.1:c.72+147G>T	ENSP00000490489.1:n.72+147G>T
ENST00000636615.1:c.1071+147G>T	ENSP00000490014.1:n.1071+147G>T
ENST00000636843.1:c.1080G>T	ENSP00000490897.1:p.Gly360=
ENST00000637158.1:n.684G>T
ENST00000637381.2:n.3514G>T
ENST00000637387.1:c.1065G>T	ENSP00000490598.1:p.Gly355=
ENST00000637815.2:c.1068G>T	ENSP00000490344.1:p.Gly356=
ENST00000637915.1:c.1077G>T	ENSP00000490471.1:p.Gly359=
ENST00000637937.1:n.394G>T
ENST00000678991.1:c.*947G>T	ENSP00000503019.1:n.*947G>T
ENST00000236671.6:c.1086G>T	ENSP00000236671.2:p.Gly362=
ENST00000427721.2:c.471+147G>T	ENSP00000415840.2:n.471+147G>T
ENST00000429746.1:c.417G>T	ENSP00000402586.1:p.Gly139=
ENST00000433655.5:c.*252G>T	ENSP00000404902.1:n.*252G>T
NM_001909.4:c.1086G>T	NP_001900.1:p.Gly362=
NM_001909.5:c.1086G>T MANE Select	NP_001900.1:p.Gly362=