Canonical Allele Identifier: CA379092608

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1774845G>T (hg19) ; chr11:g.1753615G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753615G>T , CM000673.2:g.1753615G>T	GRCh38
NC_000011.9:g.1774845G>T , CM000673.1:g.1774845G>T	GRCh37
NC_000011.8:g.1731421G>T	NCBI36
NG_008655.1:g.15378C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000236671.7:c.1127C>A MANE Select	ENSP00000236671.2:p.Pro376Gln
ENST00000367196.4:c.1022C>A	ENSP00000356164.4:p.Pro341Gln
ENST00000427721.3:c.552C>A
ENST00000429746.2:c.1022C>A	ENSP00000402586.2:p.Pro341Gln
ENST00000433655.6:c.*293C>A	ENSP00000404902.1:n.*293C>A
ENST00000438213.6:c.1244C>A	ENSP00000415036.2:p.Pro415Gln
ENST00000636397.1:c.1071+188C>A	ENSP00000489910.1:n.1071+188C>A
ENST00000636571.1:c.1106C>A	ENSP00000490770.1:p.Pro369Gln
ENST00000636579.1:c.72+188C>A	ENSP00000490489.1:n.72+188C>A
ENST00000636615.1:c.1071+188C>A	ENSP00000490014.1:n.1071+188C>A
ENST00000636843.1:c.1121C>A	ENSP00000490897.1:p.Pro374Gln
ENST00000637158.1:n.725C>A
ENST00000637381.2:n.3555C>A
ENST00000637387.1:c.1106C>A	ENSP00000490598.1:p.Pro369Gln
ENST00000637815.2:c.1109C>A	ENSP00000490344.1:p.Pro370Gln
ENST00000637915.1:c.1118C>A	ENSP00000490471.1:p.Pro373Gln
ENST00000637937.1:n.435C>A
ENST00000678991.1:c.*988C>A	ENSP00000503019.1:n.*988C>A
ENST00000236671.6:c.1127C>A	ENSP00000236671.2:p.Pro376Gln
ENST00000427721.2:c.471+188C>A	ENSP00000415840.2:n.471+188C>A
ENST00000429746.1:c.458C>A	ENSP00000402586.1:p.Pro153Gln
ENST00000433655.5:c.*293C>A	ENSP00000404902.1:n.*293C>A
NM_001909.4:c.1127C>A	NP_001900.1:p.Pro376Gln
NM_001909.5:c.1127C>A MANE Select	NP_001900.1:p.Pro376Gln