Canonical Allele Identifier: CA379098296

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1780794T>A (hg19) ; chr11:g.1759564T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1759564T>A , CM000673.2:g.1759564T>A	GRCh38
NC_000011.9:g.1780794T>A , CM000673.1:g.1780794T>A	GRCh37
NC_000011.8:g.1737370T>A	NCBI36
NG_008655.1:g.9429A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.304A>T MANE Select	ENSP00000236671.2:p.Asn102Tyr
ENST00000367196.4:c.199A>T	ENSP00000356164.4:p.Asn67Tyr
ENST00000429746.2:c.199A>T	ENSP00000402586.2:p.Asn67Tyr
ENST00000433655.6:c.304A>T	ENSP00000404902.1:p.Asn102Tyr
ENST00000438213.6:c.304A>T	ENSP00000415036.2:p.Asn102Tyr
ENST00000636397.1:c.304A>T	ENSP00000489910.1:p.Asn102Tyr
ENST00000636571.1:c.283A>T	ENSP00000490770.1:p.Asn95Tyr
ENST00000636615.1:c.304A>T	ENSP00000490014.1:p.Asn102Tyr
ENST00000636843.1:c.298A>T	ENSP00000490897.1:p.Asn100Tyr
ENST00000637381.2:n.2732A>T
ENST00000637387.1:c.304A>T	ENSP00000490598.1:p.Asn102Tyr
ENST00000637815.2:c.304A>T	ENSP00000490344.1:p.Asn102Tyr
ENST00000637915.1:c.304A>T	ENSP00000490471.1:p.Asn102Tyr
ENST00000677300.1:n.699A>T
ENST00000678991.1:c.*165A>T	ENSP00000503019.1:n.*165A>T
ENST00000236671.6:c.304A>T	ENSP00000236671.2:p.Asn102Tyr
ENST00000367196.3:c.199A>T	ENSP00000356164.3:p.Asn67Tyr
ENST00000433655.5:c.304A>T	ENSP00000404902.1:p.Asn102Tyr
ENST00000438213.5:c.259A>T	ENSP00000415036.1:p.Asn87Tyr
NM_001909.4:c.304A>T	NP_001900.1:p.Asn102Tyr
NM_001909.5:c.304A>T MANE Select	NP_001900.1:p.Asn102Tyr