Canonical Allele Identifier: CA471983610

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1776213T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1754983T>A , CM000673.2:g.1754983T>A	GRCh38
NC_000011.9:g.1776213T>A , CM000673.1:g.1776213T>A	GRCh37
NC_000011.8:g.1732789T>A	NCBI36
NG_008655.1:g.14010A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000236671.7:c.750A>T MANE Select	ENSP00000236671.2:p.Thr250=
ENST00000367196.4:c.645A>T	ENSP00000356164.4:p.Thr215=
ENST00000427721.3:c.175A>T
ENST00000429746.2:c.645A>T	ENSP00000402586.2:p.Thr215=
ENST00000433655.6:c.750A>T	ENSP00000404902.1:p.Thr250=
ENST00000438213.6:c.750A>T	ENSP00000415036.2:p.Thr250=
ENST00000497544.3:n.366A>T
ENST00000636397.1:c.750A>T	ENSP00000489910.1:p.Thr250=
ENST00000636571.1:c.729A>T	ENSP00000490770.1:p.Thr243=
ENST00000636615.1:c.750A>T	ENSP00000490014.1:p.Thr250=
ENST00000636843.1:c.744A>T	ENSP00000490897.1:p.Thr248=
ENST00000637158.1:n.348A>T
ENST00000637381.2:n.3178A>T
ENST00000637387.1:c.750A>T	ENSP00000490598.1:p.Thr250=
ENST00000637815.2:c.750A>T	ENSP00000490344.1:p.Thr250=
ENST00000637915.1:c.750A>T	ENSP00000490471.1:p.Thr250=
ENST00000637937.1:n.58A>T
ENST00000678991.1:c.*611A>T	ENSP00000503019.1:n.*611A>T
ENST00000236671.6:c.750A>T	ENSP00000236671.2:p.Thr250=
ENST00000427721.2:c.150A>T	ENSP00000415840.2:p.Thr50=
ENST00000433655.5:c.750A>T	ENSP00000404902.1:p.Thr250=
ENST00000438213.5:c.705A>T	ENSP00000415036.1:p.Thr235=
ENST00000497544.1:n.366A>T
NM_001909.4:c.750A>T	NP_001900.1:p.Thr250=
NM_001909.5:c.750A>T MANE Select	NP_001900.1:p.Thr250=