Canonical Allele Identifier: CA1947825058

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753463T= , CM000673.2:g.1753463T=	GRCh38
NC_000011.9:g.1774693T= , CM000673.1:g.1774693T=	GRCh37
NC_000011.8:g.1731269T=	NCBI36
NG_008655.1:g.15530A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000236671.7:c.*40A= MANE Select	ENSP00000236671.2:n.*40A=
ENST00000367196.4:c.*40A=	ENSP00000356164.4:n.*40A=
ENST00000427721.3:c.634+70A=
ENST00000429746.2:c.*40A=	ENSP00000402586.2:n.*40A=
ENST00000433655.6:c.*445A=	ENSP00000404902.1:n.*445A=
ENST00000438213.6:c.*40A=	ENSP00000415036.2:n.*40A=
ENST00000636397.1:c.1071+340A=	ENSP00000489910.1:n.1071+340A=
ENST00000636571.1:c.*40A=	ENSP00000490770.1:n.*40A=
ENST00000636579.1:c.72+340A=	ENSP00000490489.1:n.72+340A=
ENST00000636615.1:c.1071+340A=	ENSP00000490014.1:n.1071+340A=
ENST00000636843.1:c.*40A=	ENSP00000490897.1:n.*40A=
ENST00000637158.1:n.877A=
ENST00000637381.2:n.3707A=
ENST00000637387.1:c.*40A=	ENSP00000490598.1:n.*40A=
ENST00000637815.2:c.*40A=	ENSP00000490344.1:n.*40A=
ENST00000637915.1:c.*40A=	ENSP00000490471.1:n.*40A=
ENST00000637937.1:n.587A=
ENST00000678991.1:c.*1140A=	ENSP00000503019.1:n.*1140A=
ENST00000236671.6:c.*40A=	ENSP00000236671.2:n.*40A=
ENST00000427721.2:c.471+340A=	ENSP00000415840.2:n.471+340A=
ENST00000429746.1:c.610A=	ENSP00000402586.1:n.610A=
ENST00000433655.5:c.*445A=	ENSP00000404902.1:n.*445A=
NM_001909.4:c.*40A=	NP_001900.1:n.*40A=
NM_001909.5:c.*40A= MANE Select	NP_001900.1:n.*40A=