Canonical Allele Identifier: CA1947825060

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753466C= , CM000673.2:g.1753466C=	GRCh38
NC_000011.9:g.1774696C= , CM000673.1:g.1774696C=	GRCh37
NC_000011.8:g.1731272C=	NCBI36
NG_008655.1:g.15527G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000236671.7:c.*37G= MANE Select	ENSP00000236671.2:n.*37G=
ENST00000367196.4:c.*37G=	ENSP00000356164.4:n.*37G=
ENST00000427721.3:c.634+67G=
ENST00000429746.2:c.*37G=	ENSP00000402586.2:n.*37G=
ENST00000433655.6:c.*442G=	ENSP00000404902.1:n.*442G=
ENST00000438213.6:c.*37G=	ENSP00000415036.2:n.*37G=
ENST00000636397.1:c.1071+337G=	ENSP00000489910.1:n.1071+337G=
ENST00000636571.1:c.*37G=	ENSP00000490770.1:n.*37G=
ENST00000636579.1:c.72+337G=	ENSP00000490489.1:n.72+337G=
ENST00000636615.1:c.1071+337G=	ENSP00000490014.1:n.1071+337G=
ENST00000636843.1:c.*37G=	ENSP00000490897.1:n.*37G=
ENST00000637158.1:n.874G=
ENST00000637381.2:n.3704G=
ENST00000637387.1:c.*37G=	ENSP00000490598.1:n.*37G=
ENST00000637815.2:c.*37G=	ENSP00000490344.1:n.*37G=
ENST00000637915.1:c.*37G=	ENSP00000490471.1:n.*37G=
ENST00000637937.1:n.584G=
ENST00000678991.1:c.*1137G=	ENSP00000503019.1:n.*1137G=
ENST00000236671.6:c.*37G=	ENSP00000236671.2:n.*37G=
ENST00000427721.2:c.471+337G=	ENSP00000415840.2:n.471+337G=
ENST00000429746.1:c.607G=	ENSP00000402586.1:n.607G=
ENST00000433655.5:c.*442G=	ENSP00000404902.1:n.*442G=
NM_001909.4:c.*37G=	NP_001900.1:n.*37G=
NM_001909.5:c.*37G= MANE Select	NP_001900.1:n.*37G=