Canonical Allele Identifier: CA379099577

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1782595C>G (hg19) ; chr11:g.1761365C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1761365C>G , CM000673.2:g.1761365C>G	GRCh38
NC_000011.9:g.1782595C>G , CM000673.1:g.1782595C>G	GRCh37
NC_000011.8:g.1739171C>G	NCBI36
NG_008655.1:g.7628G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.172G>C MANE Select	ENSP00000236671.2:p.Ala58Pro
ENST00000367196.4:c.67G>C	ENSP00000356164.4:p.Ala23Pro
ENST00000429746.2:c.67G>C	ENSP00000402586.2:p.Ala23Pro
ENST00000433655.6:c.172G>C	ENSP00000404902.1:p.Ala58Pro
ENST00000438213.6:c.172G>C	ENSP00000415036.2:p.Ala58Pro
ENST00000636397.1:c.172G>C	ENSP00000489910.1:p.Ala58Pro
ENST00000636571.1:c.172G>C	ENSP00000490770.1:p.Ala58Pro
ENST00000636615.1:c.172G>C	ENSP00000490014.1:p.Ala58Pro
ENST00000636843.1:c.172G>C	ENSP00000490897.1:p.Ala58Pro
ENST00000637381.2:n.2600G>C
ENST00000637387.1:c.172G>C	ENSP00000490598.1:p.Ala58Pro
ENST00000637815.2:c.172G>C	ENSP00000490344.1:p.Ala58Pro
ENST00000637915.1:c.172G>C	ENSP00000490471.1:p.Ala58Pro
ENST00000678991.1:c.*33G>C	ENSP00000503019.1:n.*33G>C
ENST00000236671.6:c.172G>C	ENSP00000236671.2:p.Ala58Pro
ENST00000367196.3:c.67G>C	ENSP00000356164.3:p.Ala23Pro
ENST00000433655.5:c.172G>C	ENSP00000404902.1:p.Ala58Pro
ENST00000438213.5:c.127G>C	ENSP00000415036.1:p.Ala43Pro
NM_001909.4:c.172G>C	NP_001900.1:p.Ala58Pro
NM_001909.5:c.172G>C MANE Select	NP_001900.1:p.Ala58Pro