Canonical Allele Identifier: CA414522281

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148579709T>A (hg19) ; chrX:g.149498178T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498178T>A , CM000685.2:g.149498178T>A	GRCh38
NC_000023.10:g.148579709T>A , CM000685.1:g.148579709T>A	GRCh37
NC_000023.9:g.148387614T>A	NCBI36
NG_011900.3:g.12157A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.637A>T MANE Select	ENSP00000339801.6:p.Lys213Ter
ENST00000651111.1:c.4A>T	ENSP00000498395.1:p.Lys2Ter
ENST00000340855.10:c.637A>T	ENSP00000339801.6:p.Lys213Ter
ENST00000370441.8:c.637A>T	ENSP00000359470.4:p.Lys213Ter
ENST00000422081.6:c.4A>T	ENSP00000477056.1:p.Lys2Ter
ENST00000441880.1:n.114-11080A>T
ENST00000464251.5:c.563A>T	ENSP00000428980.1:n.563A>T
ENST00000466019.1:n.89A>T
ENST00000466323.5:c.637A>T	ENSP00000418264.1:p.Lys213Ter
ENST00000490775.5:n.422A>T
NM_000202.6:c.637A>T	NP_000193.1:p.Lys213Ter
NM_001166550.2:c.367A>T	NP_001160022.1:p.Lys123Ter
NM_006123.4:c.637A>T	NP_006114.1:p.Lys213Ter
NR_104128.1:n.854A>T
NM_000202.7:c.637A>T	NP_000193.1:p.Lys213Ter
NM_001166550.3:c.367A>T	NP_001160022.1:p.Lys123Ter
NM_000202.8:c.637A>T MANE Select	NP_000193.1:p.Lys213Ter
NM_001166550.4:c.367A>T	NP_001160022.1:p.Lys123Ter
NM_006123.5:c.637A>T	NP_006114.1:p.Lys213Ter
NR_104128.2:n.806A>T