Canonical Allele Identifier: CA2465004044
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149483092T= , CM000685.2:g.149483092T= GRCh38
NC_000023.10:g.148564623T= , CM000685.1:g.148564623T= GRCh37
NC_000023.9:g.148372528T= NCBI36
NG_011900.3:g.27243A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.1307A= MANE Select ENSP00000339801.6:p.Lys436=
ENST00000651111.1:c.674A= ENSP00000498395.1:p.Lys225=
ENST00000340855.10:c.1307A= ENSP00000339801.6:p.Lys436=
ENST00000422081.6:c.674A= ENSP00000477056.1:p.Lys225=
ENST00000441880.1:n.414A=
NM_000202.6:c.1307A= NP_000193.1:p.Lys436=
NM_001166550.2:c.1037A= NP_001160022.1:p.Lys346=
NM_000202.7:c.1307A= NP_000193.1:p.Lys436=
NM_001166550.3:c.1037A= NP_001160022.1:p.Lys346=
NM_000202.8:c.1307A= MANE Select NP_000193.1:p.Lys436=
NM_001166550.4:c.1037A= NP_001160022.1:p.Lys346=