Canonical Allele Identifier: CA2611924083

Gene: CTSD

Linked Data

• gnomAD v4: 11-1758889-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1758889C>A , CM000673.2:g.1758889C>A	GRCh38
NC_000011.9:g.1780119C>A , CM000673.1:g.1780119C>A	GRCh37
NC_000011.8:g.1736695C>A	NCBI36
NG_008655.1:g.10104G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000236671.7:c.471+80G>T MANE Select	ENSP00000236671.2:n.471+80G>T
ENST00000367196.4:c.366+80G>T	ENSP00000356164.4:n.366+80G>T
ENST00000429746.2:c.366+80G>T	ENSP00000402586.2:n.366+80G>T
ENST00000433655.6:c.471+80G>T	ENSP00000404902.1:n.471+80G>T
ENST00000438213.6:c.471+80G>T	ENSP00000415036.2:n.471+80G>T
ENST00000636397.1:c.471+80G>T	ENSP00000489910.1:n.471+80G>T
ENST00000636571.1:c.450+80G>T	ENSP00000490770.1:n.450+80G>T
ENST00000636615.1:c.471+80G>T	ENSP00000490014.1:n.471+80G>T
ENST00000636843.1:c.465+80G>T	ENSP00000490897.1:n.465+80G>T
ENST00000637381.2:n.2899+80G>T
ENST00000637387.1:c.471+80G>T	ENSP00000490598.1:n.471+80G>T
ENST00000637815.2:c.471+80G>T	ENSP00000490344.1:n.471+80G>T
ENST00000637915.1:c.471+80G>T	ENSP00000490471.1:n.471+80G>T
ENST00000677300.1:n.866+80G>T
ENST00000678991.1:c.*332+80G>T	ENSP00000503019.1:n.*332+80G>T
ENST00000236671.6:c.471+80G>T	ENSP00000236671.2:n.471+80G>T
ENST00000367196.3:c.366+80G>T	ENSP00000356164.3:n.366+80G>T
ENST00000427721.2:c.-130+80G>T	ENSP00000415840.2:n.-130+80G>T
ENST00000433655.5:c.471+80G>T	ENSP00000404902.1:n.471+80G>T
ENST00000438213.5:c.426+80G>T	ENSP00000415036.1:n.426+80G>T
NM_001909.4:c.471+80G>T	NP_001900.1:n.471+80G>T
NM_001909.5:c.471+80G>T MANE Select	NP_001900.1:n.471+80G>T