Canonical Allele Identifier: CA2611926791

Gene: CTSD

Linked Data

• gnomAD v4: 11-1753438-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753438G>T , CM000673.2:g.1753438G>T	GRCh38
NC_000011.9:g.1774668G>T , CM000673.1:g.1774668G>T	GRCh37
NC_000011.8:g.1731244G>T	NCBI36
NG_008655.1:g.15555C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000236671.7:c.*65C>A MANE Select	ENSP00000236671.2:n.*65C>A
ENST00000367196.4:c.*65C>A	ENSP00000356164.4:n.*65C>A
ENST00000427721.3:c.634+95C>A
ENST00000429746.2:c.*65C>A	ENSP00000402586.2:n.*65C>A
ENST00000433655.6:c.*470C>A	ENSP00000404902.1:n.*470C>A
ENST00000438213.6:c.*65C>A	ENSP00000415036.2:n.*65C>A
ENST00000636397.1:c.1071+365C>A	ENSP00000489910.1:n.1071+365C>A
ENST00000636571.1:c.*65C>A	ENSP00000490770.1:n.*65C>A
ENST00000636579.1:c.72+365C>A	ENSP00000490489.1:n.72+365C>A
ENST00000636615.1:c.1071+365C>A	ENSP00000490014.1:n.1071+365C>A
ENST00000636843.1:c.*65C>A	ENSP00000490897.1:n.*65C>A
ENST00000637158.1:n.902C>A
ENST00000637381.2:n.3732C>A
ENST00000637387.1:c.*65C>A	ENSP00000490598.1:n.*65C>A
ENST00000637815.2:c.*65C>A	ENSP00000490344.1:n.*65C>A
ENST00000637915.1:c.*65C>A	ENSP00000490471.1:n.*65C>A
ENST00000637937.1:n.612C>A
ENST00000678991.1:c.*1165C>A	ENSP00000503019.1:n.*1165C>A
ENST00000236671.6:c.*65C>A	ENSP00000236671.2:n.*65C>A
ENST00000427721.2:c.471+365C>A	ENSP00000415840.2:n.471+365C>A
ENST00000429746.1:c.635C>A	ENSP00000402586.1:n.635C>A
ENST00000433655.5:c.*470C>A	ENSP00000404902.1:n.*470C>A
NM_001909.4:c.*65C>A	NP_001900.1:n.*65C>A
NM_001909.5:c.*65C>A MANE Select	NP_001900.1:n.*65C>A