Canonical Allele Identifier: CA2465006822
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149490470G= , CM000685.2:g.149490470G= GRCh38
NC_000023.10:g.148572001G= , CM000685.1:g.148572001G= GRCh37
NC_000023.9:g.148379906G= NCBI36
NG_011900.3:g.19865C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.880-30C= MANE Select ENSP00000339801.6:n.880-30C=
ENST00000651111.1:c.247-30C= ENSP00000498395.1:n.247-30C=
ENST00000340855.10:c.880-30C= ENSP00000339801.6:n.880-30C=
ENST00000370441.8:c.880-30C= ENSP00000359470.4:n.880-30C=
ENST00000422081.6:c.247-30C= ENSP00000477056.1:n.247-30C=
ENST00000441880.1:n.114-3372C=
ENST00000464251.5:c.806-30C= ENSP00000428980.1:n.806-30C=
ENST00000466323.5:c.*71-30C= ENSP00000418264.1:n.*71-30C=
ENST00000490775.5:n.665-30C=
NM_000202.6:c.880-30C= NP_000193.1:n.880-30C=
NM_001166550.2:c.610-30C= NP_001160022.1:n.610-30C=
NM_006123.4:c.880-30C= NP_006114.1:n.880-30C=
NR_104128.1:n.1227-30C=
NM_000202.7:c.880-30C= NP_000193.1:n.880-30C=
NM_001166550.3:c.610-30C= NP_001160022.1:n.610-30C=
NM_000202.8:c.880-30C= MANE Select NP_000193.1:n.880-30C=
NM_001166550.4:c.610-30C= NP_001160022.1:n.610-30C=
NM_006123.5:c.880-30C= NP_006114.1:n.880-30C=
NR_104128.2:n.1179-30C=