Canonical Allele Identifier: CA1947825386

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1754021G= , CM000673.2:g.1754021G=	GRCh38
NC_000011.9:g.1775251G= , CM000673.1:g.1775251G=	GRCh37
NC_000011.8:g.1731827G=	NCBI36
NG_008655.1:g.14972C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.945C= MANE Select	ENSP00000236671.2:p.Ile315=
ENST00000367196.4:c.840C=	ENSP00000356164.4:p.Ile280=
ENST00000427721.3:c.370C=
ENST00000429746.2:c.840C=	ENSP00000402586.2:p.Ile280=
ENST00000433655.6:c.*111C=	ENSP00000404902.1:n.*111C=
ENST00000438213.6:c.1062C=	ENSP00000415036.2:p.Ile354=
ENST00000497544.3:n.561C=
ENST00000636397.1:c.945C=	ENSP00000489910.1:p.Ile315=
ENST00000636571.1:c.924C=	ENSP00000490770.1:p.Ile308=
ENST00000636615.1:c.945C=	ENSP00000490014.1:p.Ile315=
ENST00000636843.1:c.939C=	ENSP00000490897.1:p.Ile313=
ENST00000637158.1:n.543C=
ENST00000637381.2:n.3373C=
ENST00000637387.1:c.945C=	ENSP00000490598.1:p.Ile315=
ENST00000637815.2:c.927C=	ENSP00000490344.1:p.Ile309=
ENST00000637915.1:c.945C=	ENSP00000490471.1:p.Ile315=
ENST00000637937.1:n.253C=
ENST00000678991.1:c.*806C=	ENSP00000503019.1:n.*806C=
ENST00000236671.6:c.945C=	ENSP00000236671.2:p.Ile315=
ENST00000427721.2:c.345C=	ENSP00000415840.2:p.Ile115=
ENST00000429746.1:c.276C=	ENSP00000402586.1:p.Ile92=
ENST00000433655.5:c.*111C=	ENSP00000404902.1:n.*111C=
ENST00000497544.1:n.561C=
NM_001909.4:c.945C=	NP_001900.1:p.Ile315=
NM_001909.5:c.945C= MANE Select	NP_001900.1:p.Ile315=