Canonical Allele Identifier: CA2790162979
Gene: CTSD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1753714_1753715insAC , CM000673.2:g.1753714_1753715insAC GRCh38
NC_000011.9:g.1774944_1774945insAC , CM000673.1:g.1774944_1774945insAC GRCh37
NC_000011.8:g.1731520_1731521insAC NCBI36
NG_008655.1:g.15278_15279insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000236671.7:c.1072-45_1072-44insGT MANE Select ENSP00000236671.2:n.1072-45_1072-44insGT
ENST00000367196.4:c.967-45_967-44insGT ENSP00000356164.4:n.967-45_967-44insGT
ENST00000427721.3:c.497-45_497-44insGT
ENST00000429746.2:c.967-45_967-44insGT ENSP00000402586.2:n.967-45_967-44insGT
ENST00000433655.6:c.*238-45_*238-44insGT ENSP00000404902.1:n.*238-45_*238-44insGT
ENST00000438213.6:c.1189-45_1189-44insGT ENSP00000415036.2:n.1189-45_1189-44insGT
ENST00000497544.3:n.780-45_780-44insGT
ENST00000636397.1:c.1071+88_1071+89insGT ENSP00000489910.1:n.1071+88_1071+89insGT
ENST00000636571.1:c.1051-45_1051-44insGT ENSP00000490770.1:n.1051-45_1051-44insGT
ENST00000636579.1:c.72+88_72+89insGT ENSP00000490489.1:n.72+88_72+89insGT
ENST00000636615.1:c.1071+88_1071+89insGT ENSP00000490014.1:n.1071+88_1071+89insGT
ENST00000636843.1:c.1066-45_1066-44insGT ENSP00000490897.1:n.1066-45_1066-44insGT
ENST00000637158.1:n.670-45_670-44insGT
ENST00000637381.2:n.3500-45_3500-44insGT
ENST00000637387.1:c.1051-45_1051-44insGT ENSP00000490598.1:n.1051-45_1051-44insGT
ENST00000637815.2:c.1054-45_1054-44insGT ENSP00000490344.1:n.1054-45_1054-44insGT
ENST00000637915.1:c.1072-54_1072-53insGT ENSP00000490471.1:n.1072-54_1072-53insGT
ENST00000637937.1:n.380-45_380-44insGT
ENST00000678991.1:c.*933-45_*933-44insGT ENSP00000503019.1:n.*933-45_*933-44insGT
ENST00000236671.6:c.1072-45_1072-44insGT ENSP00000236671.2:n.1072-45_1072-44insGT
ENST00000427721.2:c.471+88_471+89insGT ENSP00000415840.2:n.471+88_471+89insGT
ENST00000429746.1:c.403-45_403-44insGT ENSP00000402586.1:n.403-45_403-44insGT
ENST00000433655.5:c.*238-45_*238-44insGT ENSP00000404902.1:n.*238-45_*238-44insGT
NM_001909.4:c.1072-45_1072-44insGT NP_001900.1:n.1072-45_1072-44insGT
NM_001909.5:c.1072-45_1072-44insGT MANE Select NP_001900.1:n.1072-45_1072-44insGT