Canonical Allele Identifier: CA2465006759
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149490311T= , CM000685.2:g.149490311T= GRCh38
NC_000023.10:g.148571842T= , CM000685.1:g.148571842T= GRCh37
NC_000023.9:g.148379747T= NCBI36
NG_011900.3:g.20024A=

Transcript Alleles

HGVS Amino-acid change
ENST00000340855.11:c.1006+3A= MANE Select ENSP00000339801.6:n.1006+3A=
ENST00000651111.1:c.373+3A= ENSP00000498395.1:n.373+3A=
ENST00000340855.10:c.1006+3A= ENSP00000339801.6:n.1006+3A=
ENST00000370441.8:c.1006+3A= ENSP00000359470.4:n.1006+3A=
ENST00000422081.6:c.373+3A= ENSP00000477056.1:n.373+3A=
ENST00000441880.1:n.114-3213A=
ENST00000464251.5:c.932+3A= ENSP00000428980.1:n.932+3A=
ENST00000466323.5:c.*197+3A= ENSP00000418264.1:n.*197+3A=
ENST00000490775.5:n.791+3A=
NM_000202.6:c.1006+3A= NP_000193.1:n.1006+3A=
NM_001166550.2:c.736+3A= NP_001160022.1:n.736+3A=
NM_006123.4:c.1006+3A= NP_006114.1:n.1006+3A=
NR_104128.1:n.1353+3A=
NM_000202.7:c.1006+3A= NP_000193.1:n.1006+3A=
NM_001166550.3:c.736+3A= NP_001160022.1:n.736+3A=
NM_000202.8:c.1006+3A= MANE Select NP_000193.1:n.1006+3A=
NM_001166550.4:c.736+3A= NP_001160022.1:n.736+3A=
NM_006123.5:c.1006+3A= NP_006114.1:n.1006+3A=
NR_104128.2:n.1305+3A=