Canonical Allele Identifier: CA2465009261
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149498308C= , CM000685.2:g.149498308C= GRCh38
NC_000023.10:g.148579839C= , CM000685.1:g.148579839C= GRCh37
NC_000023.9:g.148387744C= NCBI36
NG_011900.3:g.12027G=

Transcript Alleles

HGVS Amino-acid change
ENST00000340855.11:c.508-1G= MANE Select ENSP00000339801.6:n.508-1G=
ENST00000651111.1:c.-126-1G= ENSP00000498395.1:n.-126-1G=
ENST00000340855.10:c.508-1G= ENSP00000339801.6:n.508-1G=
ENST00000370441.8:c.508-1G= ENSP00000359470.4:n.508-1G=
ENST00000422081.6:c.-126-1G= ENSP00000477056.1:n.-126-1G=
ENST00000441880.1:n.114-11210G=
ENST00000464251.5:c.434-1G= ENSP00000428980.1:n.434-1G=
ENST00000466323.5:c.508-1G= ENSP00000418264.1:n.508-1G=
ENST00000490775.5:n.293-1G=
ENST00000523759.5:n.622-1G=
NM_000202.6:c.508-1G= NP_000193.1:n.508-1G=
NM_001166550.2:c.238-1G= NP_001160022.1:n.238-1G=
NM_006123.4:c.508-1G= NP_006114.1:n.508-1G=
NR_104128.1:n.725-1G=
NM_000202.7:c.508-1G= NP_000193.1:n.508-1G=
NM_001166550.3:c.238-1G= NP_001160022.1:n.238-1G=
NM_000202.8:c.508-1G= MANE Select NP_000193.1:n.508-1G=
NM_001166550.4:c.238-1G= NP_001160022.1:n.238-1G=
NM_006123.5:c.508-1G= NP_006114.1:n.508-1G=
NR_104128.2:n.677-1G=