Canonical Allele Identifier: CA1947834899

Gene: CTSD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1759631G= , CM000673.2:g.1759631G=	GRCh38
NC_000011.9:g.1780861G= , CM000673.1:g.1780861G=	GRCh37
NC_000011.8:g.1737437G=	NCBI36
NG_008655.1:g.9362C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.237C= MANE Select	ENSP00000236671.2:p.Tyr79=
ENST00000367196.4:c.132C=	ENSP00000356164.4:p.Tyr44=
ENST00000429746.2:c.132C=	ENSP00000402586.2:p.Tyr44=
ENST00000433655.6:c.237C=	ENSP00000404902.1:p.Tyr79=
ENST00000438213.6:c.237C=	ENSP00000415036.2:p.Tyr79=
ENST00000636397.1:c.237C=	ENSP00000489910.1:p.Tyr79=
ENST00000636571.1:c.216C=	ENSP00000490770.1:p.Tyr72=
ENST00000636615.1:c.237C=	ENSP00000490014.1:p.Tyr79=
ENST00000636843.1:c.231C=	ENSP00000490897.1:p.Tyr77=
ENST00000637381.2:n.2665C=
ENST00000637387.1:c.237C=	ENSP00000490598.1:p.Tyr79=
ENST00000637815.2:c.237C=	ENSP00000490344.1:p.Tyr79=
ENST00000637915.1:c.237C=	ENSP00000490471.1:p.Tyr79=
ENST00000677300.1:n.632C=
ENST00000678991.1:c.*98C=	ENSP00000503019.1:n.*98C=
ENST00000236671.6:c.237C=	ENSP00000236671.2:p.Tyr79=
ENST00000367196.3:c.132C=	ENSP00000356164.3:p.Tyr44=
ENST00000433655.5:c.237C=	ENSP00000404902.1:p.Tyr79=
ENST00000438213.5:c.192C=	ENSP00000415036.1:p.Tyr64=
NM_001909.4:c.237C=	NP_001900.1:p.Tyr79=
NM_001909.5:c.237C= MANE Select	NP_001900.1:p.Tyr79=