Canonical Allele Identifier: CA10537426
Community Standard Title: NM_000202.8(IDS):c.1617C>T (p.Ser539=)
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149482782G>A , CM000685.2:g.149482782G>A GRCh38
NC_000023.10:g.148564313G>A , CM000685.1:g.148564313G>A GRCh37
NC_000023.9:g.148372218G>A NCBI36
NG_011900.3:g.27553C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000202.8:c.1617C>T MANE Select NP_000193.1:p.Ser539=
ENST00000340855.11:c.1617C>T MANE Select ENSP00000339801.6:p.Ser539=
NM_000202.6:c.1617C>T NP_000193.1:p.Ser539=
NM_000202.7:c.1617C>T NP_000193.1:p.Ser539=
NM_001166550.2:c.1347C>T NP_001160022.1:p.Ser449=
NM_001166550.3:c.1347C>T NP_001160022.1:p.Ser449=
NM_001166550.4:c.1347C>T NP_001160022.1:p.Ser449=
ENST00000340855.10:c.1617C>T ENSP00000339801.6:p.Ser539=
ENST00000422081.6:c.984C>T ENSP00000477056.1:p.Ser328=
ENST00000651111.1:c.984C>T ENSP00000498395.1:p.Ser328=