Canonical Allele Identifier: CA471986211

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1778724G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1757494G>A , CM000673.2:g.1757494G>A	GRCh38
NC_000011.9:g.1778724G>A , CM000673.1:g.1778724G>A	GRCh37
NC_000011.8:g.1735300G>A	NCBI36
NG_008655.1:g.11499C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.534C>T MANE Select	ENSP00000236671.2:p.Val178=
ENST00000367196.4:c.429C>T	ENSP00000356164.4:p.Val143=
ENST00000429746.2:c.429C>T	ENSP00000402586.2:p.Val143=
ENST00000433655.6:c.534C>T	ENSP00000404902.1:p.Val178=
ENST00000438213.6:c.534C>T	ENSP00000415036.2:p.Val178=
ENST00000636397.1:c.534C>T	ENSP00000489910.1:p.Val178=
ENST00000636571.1:c.513C>T	ENSP00000490770.1:p.Val171=
ENST00000636615.1:c.534C>T	ENSP00000490014.1:p.Val178=
ENST00000636843.1:c.528C>T	ENSP00000490897.1:p.Val176=
ENST00000637158.1:n.132C>T
ENST00000637381.2:n.2962C>T
ENST00000637387.1:c.534C>T	ENSP00000490598.1:p.Val178=
ENST00000637815.2:c.534C>T	ENSP00000490344.1:p.Val178=
ENST00000637915.1:c.534C>T	ENSP00000490471.1:p.Val178=
ENST00000677300.1:n.929C>T
ENST00000678991.1:c.*395C>T	ENSP00000503019.1:n.*395C>T
ENST00000236671.6:c.534C>T	ENSP00000236671.2:p.Val178=
ENST00000367196.3:c.429C>T	ENSP00000356164.3:p.Val143=
ENST00000427721.2:c.-67C>T	ENSP00000415840.2:n.-67C>T
ENST00000433655.5:c.534C>T	ENSP00000404902.1:p.Val178=
ENST00000438213.5:c.489C>T	ENSP00000415036.1:p.Val163=
NM_001909.4:c.534C>T	NP_001900.1:p.Val178=
NM_001909.5:c.534C>T MANE Select	NP_001900.1:p.Val178=