Canonical Allele Identifier: CA379093429

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1775131A>G (hg19) ; chr11:g.1753901A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753901A>G , CM000673.2:g.1753901A>G	GRCh38
NC_000011.9:g.1775131A>G , CM000673.1:g.1775131A>G	GRCh37
NC_000011.8:g.1731707A>G	NCBI36
NG_008655.1:g.15092T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.973T>C MANE Select	ENSP00000236671.2:p.Tyr325His
ENST00000367196.4:c.868T>C	ENSP00000356164.4:p.Tyr290His
ENST00000427721.3:c.398T>C
ENST00000429746.2:c.868T>C	ENSP00000402586.2:p.Tyr290His
ENST00000433655.6:c.*139T>C	ENSP00000404902.1:n.*139T>C
ENST00000438213.6:c.1090T>C	ENSP00000415036.2:p.Tyr364His
ENST00000497544.3:n.681T>C
ENST00000636397.1:c.973T>C	ENSP00000489910.1:p.Tyr325His
ENST00000636571.1:c.952T>C	ENSP00000490770.1:p.Tyr318His
ENST00000636615.1:c.973T>C	ENSP00000490014.1:p.Tyr325His
ENST00000636843.1:c.967T>C	ENSP00000490897.1:p.Tyr323His
ENST00000637158.1:n.571T>C
ENST00000637381.2:n.3401T>C
ENST00000637387.1:c.973-21T>C	ENSP00000490598.1:n.973-21T>C
ENST00000637815.2:c.955T>C	ENSP00000490344.1:p.Tyr319His
ENST00000637915.1:c.973T>C	ENSP00000490471.1:p.Tyr325His
ENST00000637937.1:n.281T>C
ENST00000678991.1:c.*834T>C	ENSP00000503019.1:n.*834T>C
ENST00000236671.6:c.973T>C	ENSP00000236671.2:p.Tyr325His
ENST00000427721.2:c.373T>C	ENSP00000415840.2:p.Tyr125His
ENST00000429746.1:c.304T>C	ENSP00000402586.1:p.Tyr102His
ENST00000433655.5:c.*139T>C	ENSP00000404902.1:n.*139T>C
ENST00000497544.1:n.681T>C
NM_001909.4:c.973T>C	NP_001900.1:p.Tyr325His
NM_001909.5:c.973T>C MANE Select	NP_001900.1:p.Tyr325His