Canonical Allele Identifier: CA379092594

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1774840G>C (hg19) ; chr11:g.1753610G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753610G>C , CM000673.2:g.1753610G>C	GRCh38
NC_000011.9:g.1774840G>C , CM000673.1:g.1774840G>C	GRCh37
NC_000011.8:g.1731416G>C	NCBI36
NG_008655.1:g.15383C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000236671.7:c.1132C>G MANE Select	ENSP00000236671.2:p.Pro378Ala
ENST00000367196.4:c.1027C>G	ENSP00000356164.4:p.Pro343Ala
ENST00000427721.3:c.557C>G
ENST00000429746.2:c.1027C>G	ENSP00000402586.2:p.Pro343Ala
ENST00000433655.6:c.*298C>G	ENSP00000404902.1:n.*298C>G
ENST00000438213.6:c.1249C>G	ENSP00000415036.2:p.Pro417Ala
ENST00000636397.1:c.1071+193C>G	ENSP00000489910.1:n.1071+193C>G
ENST00000636571.1:c.1111C>G	ENSP00000490770.1:p.Pro371Ala
ENST00000636579.1:c.72+193C>G	ENSP00000490489.1:n.72+193C>G
ENST00000636615.1:c.1071+193C>G	ENSP00000490014.1:n.1071+193C>G
ENST00000636843.1:c.1126C>G	ENSP00000490897.1:p.Pro376Ala
ENST00000637158.1:n.730C>G
ENST00000637381.2:n.3560C>G
ENST00000637387.1:c.1111C>G	ENSP00000490598.1:p.Pro371Ala
ENST00000637815.2:c.1114C>G	ENSP00000490344.1:p.Pro372Ala
ENST00000637915.1:c.1123C>G	ENSP00000490471.1:p.Pro375Ala
ENST00000637937.1:n.440C>G
ENST00000678991.1:c.*993C>G	ENSP00000503019.1:n.*993C>G
ENST00000236671.6:c.1132C>G	ENSP00000236671.2:p.Pro378Ala
ENST00000427721.2:c.471+193C>G	ENSP00000415840.2:n.471+193C>G
ENST00000429746.1:c.463C>G	ENSP00000402586.1:p.Pro155Ala
ENST00000433655.5:c.*298C>G	ENSP00000404902.1:n.*298C>G
NM_001909.4:c.1132C>G	NP_001900.1:p.Pro378Ala
NM_001909.5:c.1132C>G MANE Select	NP_001900.1:p.Pro378Ala