Canonical Allele Identifier: CA2465003985
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149482943_149482945delinsTTA , CM000685.2:g.149482943_149482945delinsTTA GRCh38
NC_000023.10:g.148564474_148564476delinsTTA , CM000685.1:g.148564474_148564476delinsTTA GRCh37
NC_000023.9:g.148372379_148372381delinsTTA NCBI36
NG_011900.3:g.27390_27392delinsTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.1454_1456delinsTAA MANE Select ENSP00000339801.6:p.Ile485=
ENST00000651111.1:c.821_823delinsTAA ENSP00000498395.1:p.Ile274=
ENST00000340855.10:c.1454_1456delinsTAA ENSP00000339801.6:p.Ile485=
ENST00000422081.6:c.821_823delinsTAA ENSP00000477056.1:p.Ile274=
NM_000202.6:c.1454_1456delinsTAA NP_000193.1:p.Ile485=
NM_001166550.2:c.1184_1186delinsTAA NP_001160022.1:p.Ile395=
NM_000202.7:c.1454_1456delinsTAA NP_000193.1:p.Ile485=
NM_001166550.3:c.1184_1186delinsTAA NP_001160022.1:p.Ile395=
NM_000202.8:c.1454_1456delinsTAA MANE Select NP_000193.1:p.Ile485=
NM_001166550.4:c.1184_1186delinsTAA NP_001160022.1:p.Ile395=