Canonical Allele Identifier: CA1947827600

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1757402T= , CM000673.2:g.1757402T=	GRCh38
NC_000011.9:g.1778632T= , CM000673.1:g.1778632T=	GRCh37
NC_000011.8:g.1735208T=	NCBI36
NG_008655.1:g.11591A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000236671.7:c.626A= MANE Select	ENSP00000236671.2:p.Asn209=
ENST00000367196.4:c.521A=	ENSP00000356164.4:p.Asn174=
ENST00000427721.3:c.51A=
ENST00000429746.2:c.521A=	ENSP00000402586.2:p.Asn174=
ENST00000433655.6:c.626A=	ENSP00000404902.1:p.Asn209=
ENST00000438213.6:c.626A=	ENSP00000415036.2:p.Asn209=
ENST00000636397.1:c.626A=	ENSP00000489910.1:p.Asn209=
ENST00000636571.1:c.605A=	ENSP00000490770.1:p.Asn202=
ENST00000636615.1:c.626A=	ENSP00000490014.1:p.Asn209=
ENST00000636843.1:c.620A=	ENSP00000490897.1:p.Asn207=
ENST00000637158.1:n.224A=
ENST00000637381.2:n.3054A=
ENST00000637387.1:c.626A=	ENSP00000490598.1:p.Asn209=
ENST00000637815.2:c.626A=	ENSP00000490344.1:p.Asn209=
ENST00000637915.1:c.626A=	ENSP00000490471.1:p.Asn209=
ENST00000677300.1:n.1021A=
ENST00000678991.1:c.*487A=	ENSP00000503019.1:n.*487A=
ENST00000236671.6:c.626A=	ENSP00000236671.2:p.Asn209=
ENST00000367196.3:c.521A=	ENSP00000356164.3:p.Asn174=
ENST00000427721.2:c.26A=	ENSP00000415840.2:p.Asn9=
ENST00000433655.5:c.626A=	ENSP00000404902.1:p.Asn209=
ENST00000438213.5:c.581A=	ENSP00000415036.1:p.Asn194=
NM_001909.4:c.626A=	NP_001900.1:p.Asn209=
NM_001909.5:c.626A= MANE Select	NP_001900.1:p.Asn209=