Canonical Allele Identifier: CA414518029
Gene: IDS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149482934C>T , CM000685.2:g.149482934C>T GRCh38
NC_000023.10:g.148564465C>T , CM000685.1:g.148564465C>T GRCh37
NC_000023.9:g.148372370C>T NCBI36
NG_011900.3:g.27401G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000340855.11:c.1465G>A MANE Select ENSP00000339801.6:p.Gly489Ser
ENST00000651111.1:c.832G>A ENSP00000498395.1:p.Gly278Ser
ENST00000340855.10:c.1465G>A ENSP00000339801.6:p.Gly489Ser
ENST00000422081.6:c.832G>A ENSP00000477056.1:p.Gly278Ser
NM_000202.6:c.1465G>A NP_000193.1:p.Gly489Ser
NM_001166550.2:c.1195G>A NP_001160022.1:p.Gly399Ser
NM_000202.7:c.1465G>A NP_000193.1:p.Gly489Ser
NM_001166550.3:c.1195G>A NP_001160022.1:p.Gly399Ser
NM_000202.8:c.1465G>A MANE Select NP_000193.1:p.Gly489Ser
NM_001166550.4:c.1195G>A NP_001160022.1:p.Gly399Ser