Canonical Allele Identifier: CA5813968

Gene: CTSD

Linked Data

• dbSNP Id: rs750270880
• ExAC: 11:1775180 T / C
• gnomAD v4: 11-1753950-T-C
• MyVariant Identifiers: chr11:g.1775180T>C (hg19) ; chr11:g.1753950T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753950T>C , CM000673.2:g.1753950T>C	GRCh38
NC_000011.9:g.1775180T>C , CM000673.1:g.1775180T>C	GRCh37
NC_000011.8:g.1731756T>C	NCBI36
NG_008655.1:g.15043A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.972+44A>G MANE Select	ENSP00000236671.2:n.972+44A>G
ENST00000367196.4:c.867+44A>G	ENSP00000356164.4:n.867+44A>G
ENST00000427721.3:c.397+44A>G
ENST00000429746.2:c.867+44A>G	ENSP00000402586.2:n.867+44A>G
ENST00000433655.6:c.*138+44A>G	ENSP00000404902.1:n.*138+44A>G
ENST00000438213.6:c.1089+44A>G	ENSP00000415036.2:n.1089+44A>G
ENST00000497544.3:n.632A>G
ENST00000636397.1:c.972+44A>G	ENSP00000489910.1:n.972+44A>G
ENST00000636571.1:c.951+44A>G	ENSP00000490770.1:n.951+44A>G
ENST00000636615.1:c.972+44A>G	ENSP00000490014.1:n.972+44A>G
ENST00000636843.1:c.966+44A>G	ENSP00000490897.1:n.966+44A>G
ENST00000637158.1:n.570+44A>G
ENST00000637381.2:n.3400+44A>G
ENST00000637387.1:c.972+44A>G	ENSP00000490598.1:n.972+44A>G
ENST00000637815.2:c.954+44A>G	ENSP00000490344.1:n.954+44A>G
ENST00000637915.1:c.972+44A>G	ENSP00000490471.1:n.972+44A>G
ENST00000637937.1:n.280+44A>G
ENST00000678991.1:c.*833+44A>G	ENSP00000503019.1:n.*833+44A>G
ENST00000236671.6:c.972+44A>G	ENSP00000236671.2:n.972+44A>G
ENST00000427721.2:c.372+44A>G	ENSP00000415840.2:n.372+44A>G
ENST00000429746.1:c.303+44A>G	ENSP00000402586.1:n.303+44A>G
ENST00000433655.5:c.*138+44A>G	ENSP00000404902.1:n.*138+44A>G
ENST00000497544.1:n.632A>G
NM_001909.4:c.972+44A>G	NP_001900.1:n.972+44A>G
NM_001909.5:c.972+44A>G MANE Select	NP_001900.1:n.972+44A>G