Canonical Allele Identifier: CA472139359

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1774739G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753509G>C , CM000673.2:g.1753509G>C	GRCh38
NC_000011.9:g.1774739G>C , CM000673.1:g.1774739G>C	GRCh37
NC_000011.8:g.1731315G>C	NCBI36
NG_008655.1:g.15484C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000236671.7:c.1233C>G MANE Select	ENSP00000236671.2:p.Arg411=
ENST00000367196.4:c.1128C>G	ENSP00000356164.4:p.Arg376=
ENST00000427721.3:c.634+24C>G
ENST00000429746.2:c.1128C>G	ENSP00000402586.2:p.Arg376=
ENST00000433655.6:c.*399C>G	ENSP00000404902.1:n.*399C>G
ENST00000438213.6:c.1350C>G	ENSP00000415036.2:p.Arg450=
ENST00000636397.1:c.1071+294C>G	ENSP00000489910.1:n.1071+294C>G
ENST00000636571.1:c.1212C>G	ENSP00000490770.1:p.Arg404=
ENST00000636579.1:c.72+294C>G	ENSP00000490489.1:n.72+294C>G
ENST00000636615.1:c.1071+294C>G	ENSP00000490014.1:n.1071+294C>G
ENST00000636843.1:c.1227C>G	ENSP00000490897.1:p.Arg409=
ENST00000637158.1:n.831C>G
ENST00000637381.2:n.3661C>G
ENST00000637387.1:c.1212C>G	ENSP00000490598.1:p.Arg404=
ENST00000637815.2:c.1215C>G	ENSP00000490344.1:p.Arg405=
ENST00000637915.1:c.1224C>G	ENSP00000490471.1:p.Arg408=
ENST00000637937.1:n.541C>G
ENST00000678991.1:c.*1094C>G	ENSP00000503019.1:n.*1094C>G
ENST00000236671.6:c.1233C>G	ENSP00000236671.2:p.Arg411=
ENST00000427721.2:c.471+294C>G	ENSP00000415840.2:n.471+294C>G
ENST00000429746.1:c.564C>G	ENSP00000402586.1:p.Arg188=
ENST00000433655.5:c.*399C>G	ENSP00000404902.1:n.*399C>G
NM_001909.4:c.1233C>G	NP_001900.1:p.Arg411=
NM_001909.5:c.1233C>G MANE Select	NP_001900.1:p.Arg411=