Canonical Allele Identifier: CA1947834974

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1759704A= , CM000673.2:g.1759704A=	GRCh38
NC_000011.9:g.1780934A= , CM000673.1:g.1780934A=	GRCh37
NC_000011.8:g.1737510A=	NCBI36
NG_008655.1:g.9289T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.229-65T= MANE Select	ENSP00000236671.2:n.229-65T=
ENST00000367196.4:c.124-65T=	ENSP00000356164.4:n.124-65T=
ENST00000429746.2:c.124-65T=	ENSP00000402586.2:n.124-65T=
ENST00000433655.6:c.229-65T=	ENSP00000404902.1:n.229-65T=
ENST00000438213.6:c.229-65T=	ENSP00000415036.2:n.229-65T=
ENST00000636397.1:c.229-65T=	ENSP00000489910.1:n.229-65T=
ENST00000636571.1:c.208-65T=	ENSP00000490770.1:n.208-65T=
ENST00000636615.1:c.229-65T=	ENSP00000490014.1:n.229-65T=
ENST00000636843.1:c.229-71T=	ENSP00000490897.1:n.229-71T=
ENST00000637381.2:n.2657-65T=
ENST00000637387.1:c.229-65T=	ENSP00000490598.1:n.229-65T=
ENST00000637815.2:c.229-65T=	ENSP00000490344.1:n.229-65T=
ENST00000637915.1:c.229-65T=	ENSP00000490471.1:n.229-65T=
ENST00000677300.1:n.624-65T=
ENST00000678991.1:c.*90-65T=	ENSP00000503019.1:n.*90-65T=
ENST00000236671.6:c.229-65T=	ENSP00000236671.2:n.229-65T=
ENST00000367196.3:c.124-65T=	ENSP00000356164.3:n.124-65T=
ENST00000433655.5:c.229-65T=	ENSP00000404902.1:n.229-65T=
ENST00000438213.5:c.184-65T=	ENSP00000415036.1:n.184-65T=
NM_001909.4:c.229-65T=	NP_001900.1:n.229-65T=
NM_001909.5:c.229-65T= MANE Select	NP_001900.1:n.229-65T=