Canonical Allele Identifier: CA597430597

Gene: CTSD

Linked Data

• dbSNP Id: rs1206056940
• gnomAD v2: 11-1774699-C-A
• gnomAD v4: 11-1753469-C-A
• MyVariant Identifiers: chr11:g.1774699C>A (hg19) ; chr11:g.1753469C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753469C>A , CM000673.2:g.1753469C>A	GRCh38
NC_000011.9:g.1774699C>A , CM000673.1:g.1774699C>A	GRCh37
NC_000011.8:g.1731275C>A	NCBI36
NG_008655.1:g.15524G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000236671.7:c.*34G>T MANE Select	ENSP00000236671.2:n.*34G>T
ENST00000367196.4:c.*34G>T	ENSP00000356164.4:n.*34G>T
ENST00000427721.3:c.634+64G>T
ENST00000429746.2:c.*34G>T	ENSP00000402586.2:n.*34G>T
ENST00000433655.6:c.*439G>T	ENSP00000404902.1:n.*439G>T
ENST00000438213.6:c.*34G>T	ENSP00000415036.2:n.*34G>T
ENST00000636397.1:c.1071+334G>T	ENSP00000489910.1:n.1071+334G>T
ENST00000636571.1:c.*34G>T	ENSP00000490770.1:n.*34G>T
ENST00000636579.1:c.72+334G>T	ENSP00000490489.1:n.72+334G>T
ENST00000636615.1:c.1071+334G>T	ENSP00000490014.1:n.1071+334G>T
ENST00000636843.1:c.*34G>T	ENSP00000490897.1:n.*34G>T
ENST00000637158.1:n.871G>T
ENST00000637381.2:n.3701G>T
ENST00000637387.1:c.*34G>T	ENSP00000490598.1:n.*34G>T
ENST00000637815.2:c.*34G>T	ENSP00000490344.1:n.*34G>T
ENST00000637915.1:c.*34G>T	ENSP00000490471.1:n.*34G>T
ENST00000637937.1:n.581G>T
ENST00000678991.1:c.*1134G>T	ENSP00000503019.1:n.*1134G>T
ENST00000236671.6:c.*34G>T	ENSP00000236671.2:n.*34G>T
ENST00000427721.2:c.471+334G>T	ENSP00000415840.2:n.471+334G>T
ENST00000429746.1:c.604G>T	ENSP00000402586.1:n.604G>T
ENST00000433655.5:c.*439G>T	ENSP00000404902.1:n.*439G>T
NM_001909.4:c.*34G>T	NP_001900.1:n.*34G>T
NM_001909.5:c.*34G>T MANE Select	NP_001900.1:n.*34G>T