Canonical Allele Identifier: CA414517993
Gene: IDS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149482916T>G , CM000685.2:g.149482916T>G GRCh38
NC_000023.10:g.148564447T>G , CM000685.1:g.148564447T>G GRCh37
NC_000023.9:g.148372352T>G NCBI36
NG_011900.3:g.27419A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000340855.11:c.1483A>C MANE Select ENSP00000339801.6:p.Ile495Leu
ENST00000651111.1:c.850A>C ENSP00000498395.1:p.Ile284Leu
ENST00000340855.10:c.1483A>C ENSP00000339801.6:p.Ile495Leu
ENST00000422081.6:c.850A>C ENSP00000477056.1:p.Ile284Leu
NM_000202.6:c.1483A>C NP_000193.1:p.Ile495Leu
NM_001166550.2:c.1213A>C NP_001160022.1:p.Ile405Leu
NM_000202.7:c.1483A>C NP_000193.1:p.Ile495Leu
NM_001166550.3:c.1213A>C NP_001160022.1:p.Ile405Leu
NM_000202.8:c.1483A>C MANE Select NP_000193.1:p.Ile495Leu
NM_001166550.4:c.1213A>C NP_001160022.1:p.Ile405Leu