Canonical Allele Identifier: CA356677
Gene: IDS HGNC NCBI

Linked Data

dbSNP Id: rs113993951

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149483005T>A , CM000685.2:g.149483005T>A GRCh38
NC_000023.10:g.148564536T>A , CM000685.1:g.148564536T>A GRCh37
NC_000023.9:g.148372441T>A NCBI36
NG_011900.3:g.27330A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000340855.11:c.1394A>T MANE Select ENSP00000339801.6:p.Gln465Leu
ENST00000651111.1:c.761A>T ENSP00000498395.1:p.Gln254Leu
ENST00000340855.10:c.1394A>T ENSP00000339801.6:p.Gln465Leu
ENST00000422081.6:c.761A>T ENSP00000477056.1:p.Gln254Leu
NM_000202.6:c.1394A>T NP_000193.1:p.Gln465Leu
NM_001166550.2:c.1124A>T NP_001160022.1:p.Gln375Leu
NM_000202.7:c.1394A>T NP_000193.1:p.Gln465Leu
NM_001166550.3:c.1124A>T NP_001160022.1:p.Gln375Leu
NM_000202.8:c.1394A>T MANE Select NP_000193.1:p.Gln465Leu
NM_001166550.4:c.1124A>T NP_001160022.1:p.Gln375Leu