Canonical Allele Identifier: CA471985443

Gene: CTSD

Linked Data

• MyVariant Identifiers: chr11:g.1778634G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1757404G>C , CM000673.2:g.1757404G>C	GRCh38
NC_000011.9:g.1778634G>C , CM000673.1:g.1778634G>C	GRCh37
NC_000011.8:g.1735210G>C	NCBI36
NG_008655.1:g.11589C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000236671.7:c.624C>G MANE Select	ENSP00000236671.2:p.Val208=
ENST00000367196.4:c.519C>G	ENSP00000356164.4:p.Val173=
ENST00000427721.3:c.49C>G
ENST00000429746.2:c.519C>G	ENSP00000402586.2:p.Val173=
ENST00000433655.6:c.624C>G	ENSP00000404902.1:p.Val208=
ENST00000438213.6:c.624C>G	ENSP00000415036.2:p.Val208=
ENST00000636397.1:c.624C>G	ENSP00000489910.1:p.Val208=
ENST00000636571.1:c.603C>G	ENSP00000490770.1:p.Val201=
ENST00000636615.1:c.624C>G	ENSP00000490014.1:p.Val208=
ENST00000636843.1:c.618C>G	ENSP00000490897.1:p.Val206=
ENST00000637158.1:n.222C>G
ENST00000637381.2:n.3052C>G
ENST00000637387.1:c.624C>G	ENSP00000490598.1:p.Val208=
ENST00000637815.2:c.624C>G	ENSP00000490344.1:p.Val208=
ENST00000637915.1:c.624C>G	ENSP00000490471.1:p.Val208=
ENST00000677300.1:n.1019C>G
ENST00000678991.1:c.*485C>G	ENSP00000503019.1:n.*485C>G
ENST00000236671.6:c.624C>G	ENSP00000236671.2:p.Val208=
ENST00000367196.3:c.519C>G	ENSP00000356164.3:p.Val173=
ENST00000427721.2:c.24C>G	ENSP00000415840.2:p.Val8=
ENST00000433655.5:c.624C>G	ENSP00000404902.1:p.Val208=
ENST00000438213.5:c.579C>G	ENSP00000415036.1:p.Val193=
NM_001909.4:c.624C>G	NP_001900.1:p.Val208=
NM_001909.5:c.624C>G MANE Select	NP_001900.1:p.Val208=