Canonical Allele Identifier: CA2611927945

Gene: CTSD

Linked Data

• gnomAD v4: 11-1753965-C-CCCCCCCCCCCCCCCCCCCCCG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1753965_1753966insCCCCCCCCCCCCCCCCCCCCG , CM000673.2:g.1753965_1753966insCCCCCCCCCCCCCCCCCCCCG	GRCh38
NC_000011.9:g.1775195_1775196insCCCCCCCCCCCCCCCCCCCCG , CM000673.1:g.1775195_1775196insCCCCCCCCCCCCCCCCCCCCG	GRCh37
NC_000011.8:g.1731771_1731772insCCCCCCCCCCCCCCCCCCCCG	NCBI36
NG_008655.1:g.15027_15028insCGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236671.7:c.972+28_972+29insCGGGGGGGGGGGGGGGGGGGG MANE Select	ENSP00000236671.2:n.972+28_972+29insCGGGGGGGGGGGGGGGGGGGG
ENST00000367196.4:c.867+28_867+29insCGGGGGGGGGGGGGGGGGGGG	ENSP00000356164.4:n.867+28_867+29insCGGGGGGGGGGGGGGGGGGGG
ENST00000427721.3:c.397+28_397+29insCGGGGGGGGGGGGGGGGGGGG
ENST00000429746.2:c.867+28_867+29insCGGGGGGGGGGGGGGGGGGGG	ENSP00000402586.2:n.867+28_867+29insCGGGGGGGGGGGGGGGGGGGG
ENST00000433655.6:c.*138+28_*138+29insCGGGGGGGGGGGGGGGGGGGG	ENSP00000404902.1:n.*138+28_*138+29insCGGGGGGGGGGGGGGGGGGGG
ENST00000438213.6:c.1089+28_1089+29insCGGGGGGGGGGGGGGGGGGGG	ENSP00000415036.2:n.1089+28_1089+29insCGGGGGGGGGGGGGGGGGGGG
ENST00000497544.3:n.616_617insCGGGGGGGGGGGGGGGGGGGG
ENST00000636397.1:c.972+28_972+29insCGGGGGGGGGGGGGGGGGGGG	ENSP00000489910.1:n.972+28_972+29insCGGGGGGGGGGGGGGGGGGGG
ENST00000636571.1:c.951+28_951+29insCGGGGGGGGGGGGGGGGGGGG	ENSP00000490770.1:n.951+28_951+29insCGGGGGGGGGGGGGGGGGGGG
ENST00000636615.1:c.972+28_972+29insCGGGGGGGGGGGGGGGGGGGG	ENSP00000490014.1:n.972+28_972+29insCGGGGGGGGGGGGGGGGGGGG
ENST00000636843.1:c.966+28_966+29insCGGGGGGGGGGGGGGGGGGGG	ENSP00000490897.1:n.966+28_966+29insCGGGGGGGGGGGGGGGGGGGG
ENST00000637158.1:n.570+28_570+29insCGGGGGGGGGGGGGGGGGGGG
ENST00000637381.2:n.3400+28_3400+29insCGGGGGGGGGGGGGGGGGGGG
ENST00000637387.1:c.972+28_972+29insCGGGGGGGGGGGGGGGGGGGG	ENSP00000490598.1:n.972+28_972+29insCGGGGGGGGGGGGGGGGGGGG
ENST00000637815.2:c.954+28_954+29insCGGGGGGGGGGGGGGGGGGGG	ENSP00000490344.1:n.954+28_954+29insCGGGGGGGGGGGGGGGGGGGG
ENST00000637915.1:c.972+28_972+29insCGGGGGGGGGGGGGGGGGGGG	ENSP00000490471.1:n.972+28_972+29insCGGGGGGGGGGGGGGGGGGGG
ENST00000637937.1:n.280+28_280+29insCGGGGGGGGGGGGGGGGGGGG
ENST00000678991.1:c.*833+28_*833+29insCGGGGGGGGGGGGGGGGGGGG	ENSP00000503019.1:n.*833+28_*833+29insCGGGGGGGGGGGGGGGGGGGG
ENST00000236671.6:c.972+28_972+29insCGGGGGGGGGGGGGGGGGGGG	ENSP00000236671.2:n.972+28_972+29insCGGGGGGGGGGGGGGGGGGGG
ENST00000427721.2:c.372+28_372+29insCGGGGGGGGGGGGGGGGGGGG	ENSP00000415840.2:n.372+28_372+29insCGGGGGGGGGGGGGGGGGGGG
ENST00000429746.1:c.303+28_303+29insCGGGGGGGGGGGGGGGGGGGG	ENSP00000402586.1:n.303+28_303+29insCGGGGGGGGGGGGGGGGGGGG
ENST00000433655.5:c.*138+28_*138+29insCGGGGGGGGGGGGGGGGGGGG	ENSP00000404902.1:n.*138+28_*138+29insCGGGGGGGGGGGGGGGGGGGG
ENST00000497544.1:n.616_617insCGGGGGGGGGGGGGGGGGGGG
NM_001909.4:c.972+28_972+29insCGGGGGGGGGGGGGGGGGGGG	NP_001900.1:n.972+28_972+29insCGGGGGGGGGGGGGGGGGGGG
NM_001909.5:c.972+28_972+29insCGGGGGGGGGGGGGGGGGGGG MANE Select	NP_001900.1:n.972+28_972+29insCGGGGGGGGGGGGGGGGGGGG