Canonical Allele Identifier: CA2694909068

Gene: IDS

Linked Data

• gnomAD v4: X-149486886-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149486886T>A , CM000685.2:g.149486886T>A	GRCh38
NC_000023.10:g.148568417T>A , CM000685.1:g.148568417T>A	GRCh37
NC_000023.9:g.148376322T>A	NCBI36
NG_011900.3:g.23449A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1180+39A>T MANE Select	ENSP00000339801.6:n.1180+39A>T
ENST00000651111.1:c.547+39A>T	ENSP00000498395.1:n.547+39A>T
ENST00000340855.10:c.1180+39A>T	ENSP00000339801.6:n.1180+39A>T
ENST00000422081.6:c.547+39A>T	ENSP00000477056.1:n.547+39A>T
ENST00000441880.1:n.287+39A>T
NM_000202.6:c.1180+39A>T	NP_000193.1:n.1180+39A>T
NM_001166550.2:c.910+39A>T	NP_001160022.1:n.910+39A>T
NM_000202.7:c.1180+39A>T	NP_000193.1:n.1180+39A>T
NM_001166550.3:c.910+39A>T	NP_001160022.1:n.910+39A>T
NM_000202.8:c.1180+39A>T MANE Select	NP_000193.1:n.1180+39A>T
NM_001166550.4:c.910+39A>T	NP_001160022.1:n.910+39A>T