Canonical Allele Identifier: CA674232500

Gene: CTSD

Linked Data

• dbSNP Id: rs771305068
• gnomAD v3: 11-1753910-G-C
• gnomAD v4: 11-1753910-G-C
• MyVariant Identifiers: chr11:g.1775140G>C (hg19) ; chr11:g.1753910G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753910G>C , CM000673.2:g.1753910G>C	GRCh38
NC_000011.9:g.1775140G>C , CM000673.1:g.1775140G>C	GRCh37
NC_000011.8:g.1731716G>C	NCBI36
NG_008655.1:g.15083C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.973-9C>G MANE Select	ENSP00000236671.2:n.973-9C>G
ENST00000367196.4:c.868-9C>G	ENSP00000356164.4:n.868-9C>G
ENST00000427721.3:c.398-9C>G
ENST00000429746.2:c.868-9C>G	ENSP00000402586.2:n.868-9C>G
ENST00000433655.6:c.*139-9C>G	ENSP00000404902.1:n.*139-9C>G
ENST00000438213.6:c.1090-9C>G	ENSP00000415036.2:n.1090-9C>G
ENST00000497544.3:n.672C>G
ENST00000636397.1:c.973-9C>G	ENSP00000489910.1:n.973-9C>G
ENST00000636571.1:c.952-9C>G	ENSP00000490770.1:n.952-9C>G
ENST00000636615.1:c.973-9C>G	ENSP00000490014.1:n.973-9C>G
ENST00000636843.1:c.967-9C>G	ENSP00000490897.1:n.967-9C>G
ENST00000637158.1:n.571-9C>G
ENST00000637381.2:n.3401-9C>G
ENST00000637387.1:c.973-30C>G	ENSP00000490598.1:n.973-30C>G
ENST00000637815.2:c.955-9C>G	ENSP00000490344.1:n.955-9C>G
ENST00000637915.1:c.973-9C>G	ENSP00000490471.1:n.973-9C>G
ENST00000637937.1:n.281-9C>G
ENST00000678991.1:c.*834-9C>G	ENSP00000503019.1:n.*834-9C>G
ENST00000236671.6:c.973-9C>G	ENSP00000236671.2:n.973-9C>G
ENST00000427721.2:c.373-9C>G	ENSP00000415840.2:n.373-9C>G
ENST00000429746.1:c.304-9C>G	ENSP00000402586.1:n.304-9C>G
ENST00000433655.5:c.*139-9C>G	ENSP00000404902.1:n.*139-9C>G
ENST00000497544.1:n.672C>G
NM_001909.4:c.973-9C>G	NP_001900.1:n.973-9C>G
NM_001909.5:c.973-9C>G MANE Select	NP_001900.1:n.973-9C>G