Canonical Allele Identifier: CA2611926773

Gene: CTSD

Linked Data

• gnomAD v4: 11-1753429-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753429G>T , CM000673.2:g.1753429G>T	GRCh38
NC_000011.9:g.1774659G>T , CM000673.1:g.1774659G>T	GRCh37
NC_000011.8:g.1731235G>T	NCBI36
NG_008655.1:g.15564C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.*74C>A MANE Select	ENSP00000236671.2:n.*74C>A
ENST00000367196.4:c.*74C>A	ENSP00000356164.4:n.*74C>A
ENST00000427721.3:c.634+104C>A
ENST00000429746.2:c.*74C>A	ENSP00000402586.2:n.*74C>A
ENST00000433655.6:c.*479C>A	ENSP00000404902.1:n.*479C>A
ENST00000438213.6:c.*74C>A	ENSP00000415036.2:n.*74C>A
ENST00000636397.1:c.1071+374C>A	ENSP00000489910.1:n.1071+374C>A
ENST00000636571.1:c.*74C>A	ENSP00000490770.1:n.*74C>A
ENST00000636579.1:c.72+374C>A	ENSP00000490489.1:n.72+374C>A
ENST00000636615.1:c.1071+374C>A	ENSP00000490014.1:n.1071+374C>A
ENST00000636843.1:c.*74C>A	ENSP00000490897.1:n.*74C>A
ENST00000637158.1:n.911C>A
ENST00000637381.2:n.3741C>A
ENST00000637387.1:c.*74C>A	ENSP00000490598.1:n.*74C>A
ENST00000637815.2:c.*74C>A	ENSP00000490344.1:n.*74C>A
ENST00000637915.1:c.*74C>A	ENSP00000490471.1:n.*74C>A
ENST00000637937.1:n.621C>A
ENST00000678991.1:c.*1174C>A	ENSP00000503019.1:n.*1174C>A
ENST00000236671.6:c.*74C>A	ENSP00000236671.2:n.*74C>A
ENST00000427721.2:c.471+374C>A	ENSP00000415840.2:n.471+374C>A
ENST00000429746.1:c.644C>A	ENSP00000402586.1:n.644C>A
ENST00000433655.5:c.*479C>A	ENSP00000404902.1:n.*479C>A
NM_001909.4:c.*74C>A	NP_001900.1:n.*74C>A
NM_001909.5:c.*74C>A MANE Select	NP_001900.1:n.*74C>A