Canonical Allele Identifier: CA379092386

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1774774C>G (hg19) ; chr11:g.1753544C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753544C>G , CM000673.2:g.1753544C>G	GRCh38
NC_000011.9:g.1774774C>G , CM000673.1:g.1774774C>G	GRCh37
NC_000011.8:g.1731350C>G	NCBI36
NG_008655.1:g.15449G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1198G>C MANE Select	ENSP00000236671.2:p.Asp400His
ENST00000367196.4:c.1093G>C	ENSP00000356164.4:p.Asp365His
ENST00000427721.3:c.623G>C
ENST00000429746.2:c.1093G>C	ENSP00000402586.2:p.Asp365His
ENST00000433655.6:c.*364G>C	ENSP00000404902.1:n.*364G>C
ENST00000438213.6:c.1315G>C	ENSP00000415036.2:p.Asp439His
ENST00000636397.1:c.1071+259G>C	ENSP00000489910.1:n.1071+259G>C
ENST00000636571.1:c.1177G>C	ENSP00000490770.1:p.Asp393His
ENST00000636579.1:c.72+259G>C	ENSP00000490489.1:n.72+259G>C
ENST00000636615.1:c.1071+259G>C	ENSP00000490014.1:n.1071+259G>C
ENST00000636843.1:c.1192G>C	ENSP00000490897.1:p.Asp398His
ENST00000637158.1:n.796G>C
ENST00000637381.2:n.3626G>C
ENST00000637387.1:c.1177G>C	ENSP00000490598.1:p.Asp393His
ENST00000637815.2:c.1180G>C	ENSP00000490344.1:p.Asp394His
ENST00000637915.1:c.1189G>C	ENSP00000490471.1:p.Asp397His
ENST00000637937.1:n.506G>C
ENST00000678991.1:c.*1059G>C	ENSP00000503019.1:n.*1059G>C
ENST00000236671.6:c.1198G>C	ENSP00000236671.2:p.Asp400His
ENST00000427721.2:c.471+259G>C	ENSP00000415840.2:n.471+259G>C
ENST00000429746.1:c.529G>C	ENSP00000402586.1:p.Asp177His
ENST00000433655.5:c.*364G>C	ENSP00000404902.1:n.*364G>C
NM_001909.4:c.1198G>C	NP_001900.1:p.Asp400His
NM_001909.5:c.1198G>C MANE Select	NP_001900.1:p.Asp400His