Canonical Allele Identifier: CA597430617

Gene: CTSD

Linked Data

• dbSNP Id: rs1445599763
• gnomAD v2: 11-1775182-C-T
• gnomAD v4: 11-1753952-C-T
• MyVariant Identifiers: chr11:g.1775182C>T (hg19) ; chr11:g.1753952C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753952C>T , CM000673.2:g.1753952C>T	GRCh38
NC_000011.9:g.1775182C>T , CM000673.1:g.1775182C>T	GRCh37
NC_000011.8:g.1731758C>T	NCBI36
NG_008655.1:g.15041G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.972+42G>A MANE Select	ENSP00000236671.2:n.972+42G>A
ENST00000367196.4:c.867+42G>A	ENSP00000356164.4:n.867+42G>A
ENST00000427721.3:c.397+42G>A
ENST00000429746.2:c.867+42G>A	ENSP00000402586.2:n.867+42G>A
ENST00000433655.6:c.*138+42G>A	ENSP00000404902.1:n.*138+42G>A
ENST00000438213.6:c.1089+42G>A	ENSP00000415036.2:n.1089+42G>A
ENST00000497544.3:n.630G>A
ENST00000636397.1:c.972+42G>A	ENSP00000489910.1:n.972+42G>A
ENST00000636571.1:c.951+42G>A	ENSP00000490770.1:n.951+42G>A
ENST00000636615.1:c.972+42G>A	ENSP00000490014.1:n.972+42G>A
ENST00000636843.1:c.966+42G>A	ENSP00000490897.1:n.966+42G>A
ENST00000637158.1:n.570+42G>A
ENST00000637381.2:n.3400+42G>A
ENST00000637387.1:c.972+42G>A	ENSP00000490598.1:n.972+42G>A
ENST00000637815.2:c.954+42G>A	ENSP00000490344.1:n.954+42G>A
ENST00000637915.1:c.972+42G>A	ENSP00000490471.1:n.972+42G>A
ENST00000637937.1:n.280+42G>A
ENST00000678991.1:c.*833+42G>A	ENSP00000503019.1:n.*833+42G>A
ENST00000236671.6:c.972+42G>A	ENSP00000236671.2:n.972+42G>A
ENST00000427721.2:c.372+42G>A	ENSP00000415840.2:n.372+42G>A
ENST00000429746.1:c.303+42G>A	ENSP00000402586.1:n.303+42G>A
ENST00000433655.5:c.*138+42G>A	ENSP00000404902.1:n.*138+42G>A
ENST00000497544.1:n.630G>A
NM_001909.4:c.972+42G>A	NP_001900.1:n.972+42G>A
NM_001909.5:c.972+42G>A MANE Select	NP_001900.1:n.972+42G>A