Canonical Allele Identifier: CA414517946
Community Standard Title: NM_000202.8(IDS):c.1505G>A (p.Trp502Ter)
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149482894C>T , CM000685.2:g.149482894C>T GRCh38
NC_000023.10:g.148564425C>T , CM000685.1:g.148564425C>T GRCh37
NC_000023.9:g.148372330C>T NCBI36
NG_011900.3:g.27441G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000202.8:c.1505G>A MANE Select NP_000193.1:p.Trp502Ter
ENST00000340855.11:c.1505G>A MANE Select ENSP00000339801.6:p.Trp502Ter
NM_000202.6:c.1505G>A NP_000193.1:p.Trp502Ter
NM_000202.7:c.1505G>A NP_000193.1:p.Trp502Ter
NM_001166550.2:c.1235G>A NP_001160022.1:p.Trp412Ter
NM_001166550.3:c.1235G>A NP_001160022.1:p.Trp412Ter
NM_001166550.4:c.1235G>A NP_001160022.1:p.Trp412Ter
ENST00000340855.10:c.1505G>A ENSP00000339801.6:p.Trp502Ter
ENST00000422081.6:c.872G>A ENSP00000477056.1:p.Trp291Ter
ENST00000651111.1:c.872G>A ENSP00000498395.1:p.Trp291Ter