Canonical Allele Identifier: CA472139658

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1774769G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753539G>A , CM000673.2:g.1753539G>A	GRCh38
NC_000011.9:g.1774769G>A , CM000673.1:g.1774769G>A	GRCh37
NC_000011.8:g.1731345G>A	NCBI36
NG_008655.1:g.15454C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.1203C>T MANE Select	ENSP00000236671.2:p.Asn401=
ENST00000367196.4:c.1098C>T	ENSP00000356164.4:p.Asn366=
ENST00000427721.3:c.628C>T
ENST00000429746.2:c.1098C>T	ENSP00000402586.2:p.Asn366=
ENST00000433655.6:c.*369C>T	ENSP00000404902.1:n.*369C>T
ENST00000438213.6:c.1320C>T	ENSP00000415036.2:p.Asn440=
ENST00000636397.1:c.1071+264C>T	ENSP00000489910.1:n.1071+264C>T
ENST00000636571.1:c.1182C>T	ENSP00000490770.1:p.Asn394=
ENST00000636579.1:c.72+264C>T	ENSP00000490489.1:n.72+264C>T
ENST00000636615.1:c.1071+264C>T	ENSP00000490014.1:n.1071+264C>T
ENST00000636843.1:c.1197C>T	ENSP00000490897.1:p.Asn399=
ENST00000637158.1:n.801C>T
ENST00000637381.2:n.3631C>T
ENST00000637387.1:c.1182C>T	ENSP00000490598.1:p.Asn394=
ENST00000637815.2:c.1185C>T	ENSP00000490344.1:p.Asn395=
ENST00000637915.1:c.1194C>T	ENSP00000490471.1:p.Asn398=
ENST00000637937.1:n.511C>T
ENST00000678991.1:c.*1064C>T	ENSP00000503019.1:n.*1064C>T
ENST00000236671.6:c.1203C>T	ENSP00000236671.2:p.Asn401=
ENST00000427721.2:c.471+264C>T	ENSP00000415840.2:n.471+264C>T
ENST00000429746.1:c.534C>T	ENSP00000402586.1:p.Asn178=
ENST00000433655.5:c.*369C>T	ENSP00000404902.1:n.*369C>T
NM_001909.4:c.1203C>T	NP_001900.1:p.Asn401=
NM_001909.5:c.1203C>T MANE Select	NP_001900.1:p.Asn401=