Canonical Allele Identifier: CA2465004014
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149483011T= , CM000685.2:g.149483011T= GRCh38
NC_000023.10:g.148564542T= , CM000685.1:g.148564542T= GRCh37
NC_000023.9:g.148372447T= NCBI36
NG_011900.3:g.27324A=

Transcript Alleles

HGVS Amino-acid change
ENST00000340855.11:c.1388A= MANE Select ENSP00000339801.6:p.Tyr463=
ENST00000651111.1:c.755A= ENSP00000498395.1:p.Tyr252=
ENST00000340855.10:c.1388A= ENSP00000339801.6:p.Tyr463=
ENST00000422081.6:c.755A= ENSP00000477056.1:p.Tyr252=
NM_000202.6:c.1388A= NP_000193.1:p.Tyr463=
NM_001166550.2:c.1118A= NP_001160022.1:p.Tyr373=
NM_000202.7:c.1388A= NP_000193.1:p.Tyr463=
NM_001166550.3:c.1118A= NP_001160022.1:p.Tyr373=
NM_000202.8:c.1388A= MANE Select NP_000193.1:p.Tyr463=
NM_001166550.4:c.1118A= NP_001160022.1:p.Tyr373=