Canonical Allele Identifier: CA379099515

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1782580T>C (hg19) ; chr11:g.1761350T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1761350T>C , CM000673.2:g.1761350T>C	GRCh38
NC_000011.9:g.1782580T>C , CM000673.1:g.1782580T>C	GRCh37
NC_000011.8:g.1739156T>C	NCBI36
NG_008655.1:g.7643A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.187A>G MANE Select	ENSP00000236671.2:p.Thr63Ala
ENST00000367196.4:c.82A>G	ENSP00000356164.4:p.Thr28Ala
ENST00000429746.2:c.82A>G	ENSP00000402586.2:p.Thr28Ala
ENST00000433655.6:c.187A>G	ENSP00000404902.1:p.Thr63Ala
ENST00000438213.6:c.187A>G	ENSP00000415036.2:p.Thr63Ala
ENST00000636397.1:c.187A>G	ENSP00000489910.1:p.Thr63Ala
ENST00000636571.1:c.187A>G	ENSP00000490770.1:p.Thr63Ala
ENST00000636615.1:c.187A>G	ENSP00000490014.1:p.Thr63Ala
ENST00000636843.1:c.187A>G	ENSP00000490897.1:p.Thr63Ala
ENST00000637381.2:n.2615A>G
ENST00000637387.1:c.187A>G	ENSP00000490598.1:p.Thr63Ala
ENST00000637815.2:c.187A>G	ENSP00000490344.1:p.Thr63Ala
ENST00000637915.1:c.187A>G	ENSP00000490471.1:p.Thr63Ala
ENST00000678991.1:c.*48A>G	ENSP00000503019.1:n.*48A>G
ENST00000236671.6:c.187A>G	ENSP00000236671.2:p.Thr63Ala
ENST00000367196.3:c.82A>G	ENSP00000356164.3:p.Thr28Ala
ENST00000433655.5:c.187A>G	ENSP00000404902.1:p.Thr63Ala
ENST00000438213.5:c.142A>G	ENSP00000415036.1:p.Thr48Ala
NM_001909.4:c.187A>G	NP_001900.1:p.Thr63Ala
NM_001909.5:c.187A>G MANE Select	NP_001900.1:p.Thr63Ala