Canonical Allele Identifier: CA379097205

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1780210C>A (hg19) ; chr11:g.1758980C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1758980C>A , CM000673.2:g.1758980C>A	GRCh38
NC_000011.9:g.1780210C>A , CM000673.1:g.1780210C>A	GRCh37
NC_000011.8:g.1736786C>A	NCBI36
NG_008655.1:g.10013G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000236671.7:c.460G>T MANE Select	ENSP00000236671.2:p.Asp154Tyr
ENST00000367196.4:c.355G>T	ENSP00000356164.4:p.Asp119Tyr
ENST00000429746.2:c.355G>T	ENSP00000402586.2:p.Asp119Tyr
ENST00000433655.6:c.460G>T	ENSP00000404902.1:p.Asp154Tyr
ENST00000438213.6:c.460G>T	ENSP00000415036.2:p.Asp154Tyr
ENST00000636397.1:c.460G>T	ENSP00000489910.1:p.Asp154Tyr
ENST00000636571.1:c.439G>T	ENSP00000490770.1:p.Asp147Tyr
ENST00000636615.1:c.460G>T	ENSP00000490014.1:p.Asp154Tyr
ENST00000636843.1:c.454G>T	ENSP00000490897.1:p.Asp152Tyr
ENST00000637381.2:n.2888G>T
ENST00000637387.1:c.460G>T	ENSP00000490598.1:p.Asp154Tyr
ENST00000637815.2:c.460G>T	ENSP00000490344.1:p.Asp154Tyr
ENST00000637915.1:c.460G>T	ENSP00000490471.1:p.Asp154Tyr
ENST00000677300.1:n.855G>T
ENST00000678991.1:c.*321G>T	ENSP00000503019.1:n.*321G>T
ENST00000236671.6:c.460G>T	ENSP00000236671.2:p.Asp154Tyr
ENST00000367196.3:c.355G>T	ENSP00000356164.3:p.Asp119Tyr
ENST00000427721.2:c.-141G>T	ENSP00000415840.2:n.-141G>T
ENST00000433655.5:c.460G>T	ENSP00000404902.1:p.Asp154Tyr
ENST00000438213.5:c.415G>T	ENSP00000415036.1:p.Asp139Tyr
NM_001909.4:c.460G>T	NP_001900.1:p.Asp154Tyr
NM_001909.5:c.460G>T MANE Select	NP_001900.1:p.Asp154Tyr