Canonical Allele Identifier: CA471982939

Gene: CTSD

Linked Data

• gnomAD v4: 11-1753309-C-A
• MyVariant Identifiers: chr11:g.1774539C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753309C>A , CM000673.2:g.1753309C>A	GRCh38
NC_000011.9:g.1774539C>A , CM000673.1:g.1774539C>A	GRCh37
NC_000011.8:g.1731115C>A	NCBI36
NG_008655.1:g.15684G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.*194G>T MANE Select	ENSP00000236671.2:n.*194G>T
ENST00000367196.4:c.*194G>T	ENSP00000356164.4:n.*194G>T
ENST00000427721.3:c.634+224G>T
ENST00000429746.2:c.*194G>T	ENSP00000402586.2:n.*194G>T
ENST00000433655.6:c.*599G>T	ENSP00000404902.1:n.*599G>T
ENST00000636397.1:c.1071+494G>T	ENSP00000489910.1:n.1071+494G>T
ENST00000636571.1:c.*194G>T	ENSP00000490770.1:n.*194G>T
ENST00000636579.1:c.72+494G>T	ENSP00000490489.1:n.72+494G>T
ENST00000636615.1:c.1071+494G>T	ENSP00000490014.1:n.1071+494G>T
ENST00000637158.1:n.1031G>T
ENST00000637381.2:n.3861G>T
ENST00000637387.1:c.*194G>T	ENSP00000490598.1:n.*194G>T
ENST00000637815.2:c.*194G>T	ENSP00000490344.1:n.*194G>T
ENST00000637915.1:c.*194G>T	ENSP00000490471.1:n.*194G>T
ENST00000637937.1:n.741G>T
ENST00000678991.1:c.*1294G>T	ENSP00000503019.1:n.*1294G>T
ENST00000236671.6:c.*194G>T	ENSP00000236671.2:n.*194G>T
ENST00000427721.2:c.471+494G>T	ENSP00000415840.2:n.471+494G>T
ENST00000433655.5:c.*599G>T	ENSP00000404902.1:n.*599G>T
NM_001909.4:c.*194G>T	NP_001900.1:n.*194G>T
NM_001909.5:c.*194G>T MANE Select	NP_001900.1:n.*194G>T