Canonical Allele Identifier: CA519057380

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149482776A>C , CM000685.2:g.149482776A>C	GRCh38
NC_000023.10:g.148564307A>C , CM000685.1:g.148564307A>C	GRCh37
NC_000023.9:g.148372212A>C	NCBI36
NG_011900.3:g.27559T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000202.8:c.1623T>G MANE Select	NP_000193.1:p.Gly541=
ENST00000340855.11:c.1623T>G MANE Select	ENSP00000339801.6:p.Gly541=
NM_000202.6:c.1623T>G	NP_000193.1:p.Gly541=
NM_000202.7:c.1623T>G	NP_000193.1:p.Gly541=
NM_001166550.2:c.1353T>G	NP_001160022.1:p.Gly451=
NM_001166550.3:c.1353T>G	NP_001160022.1:p.Gly451=
NM_001166550.4:c.1353T>G	NP_001160022.1:p.Gly451=
ENST00000340855.10:c.1623T>G	ENSP00000339801.6:p.Gly541=
ENST00000422081.6:c.990T>G	ENSP00000477056.1:p.Gly330=
ENST00000651111.1:c.990T>G	ENSP00000498395.1:p.Gly330=