Canonical Allele Identifier: CA379093518

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1775230C>G (hg19) ; chr11:g.1754000C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1754000C>G , CM000673.2:g.1754000C>G	GRCh38
NC_000011.9:g.1775230C>G , CM000673.1:g.1775230C>G	GRCh37
NC_000011.8:g.1731806C>G	NCBI36
NG_008655.1:g.14993G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.966G>C MANE Select	ENSP00000236671.2:p.Gln322His
ENST00000367196.4:c.861G>C	ENSP00000356164.4:p.Gln287His
ENST00000427721.3:c.391G>C
ENST00000429746.2:c.861G>C	ENSP00000402586.2:p.Gln287His
ENST00000433655.6:c.*132G>C	ENSP00000404902.1:n.*132G>C
ENST00000438213.6:c.1083G>C	ENSP00000415036.2:p.Gln361His
ENST00000497544.3:n.582G>C
ENST00000636397.1:c.966G>C	ENSP00000489910.1:p.Gln322His
ENST00000636571.1:c.945G>C	ENSP00000490770.1:p.Gln315His
ENST00000636615.1:c.966G>C	ENSP00000490014.1:p.Gln322His
ENST00000636843.1:c.960G>C	ENSP00000490897.1:p.Gln320His
ENST00000637158.1:n.564G>C
ENST00000637381.2:n.3394G>C
ENST00000637387.1:c.966G>C	ENSP00000490598.1:p.Gln322His
ENST00000637815.2:c.948G>C	ENSP00000490344.1:p.Gln316His
ENST00000637915.1:c.966G>C	ENSP00000490471.1:p.Gln322His
ENST00000637937.1:n.274G>C
ENST00000678991.1:c.*827G>C	ENSP00000503019.1:n.*827G>C
ENST00000236671.6:c.966G>C	ENSP00000236671.2:p.Gln322His
ENST00000427721.2:c.366G>C	ENSP00000415840.2:p.Gln122His
ENST00000429746.1:c.297G>C	ENSP00000402586.1:p.Gln99His
ENST00000433655.5:c.*132G>C	ENSP00000404902.1:n.*132G>C
ENST00000497544.1:n.582G>C
NM_001909.4:c.966G>C	NP_001900.1:p.Gln322His
NM_001909.5:c.966G>C MANE Select	NP_001900.1:p.Gln322His