Canonical Allele Identifier: CA2695236487

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149482936_149482937insC , CM000685.2:g.149482936_149482937insC	GRCh38
NC_000023.10:g.148564467_148564468insC , CM000685.1:g.148564467_148564468insC	GRCh37
NC_000023.9:g.148372372_148372373insC	NCBI36
NG_011900.3:g.27398_27399insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000340855.11:c.1462_1463insG MANE Select	ENSP00000339801.6:p.Met488SerfsTer11
ENST00000651111.1:c.829_830insG	ENSP00000498395.1:p.Met277SerfsTer11
ENST00000340855.10:c.1462_1463insG	ENSP00000339801.6:p.Met488SerfsTer11
ENST00000422081.6:c.829_830insG	ENSP00000477056.1:p.Met277SerfsTer11
NM_000202.6:c.1462_1463insG	NP_000193.1:p.Met488SerfsTer11
NM_001166550.2:c.1192_1193insG	NP_001160022.1:p.Met398SerfsTer11
NM_000202.7:c.1462_1463insG	NP_000193.1:p.Met488SerfsTer11
NM_001166550.3:c.1192_1193insG	NP_001160022.1:p.Met398SerfsTer11
NM_000202.8:c.1462_1463insG MANE Select	NP_000193.1:p.Met488SerfsTer11
NM_001166550.4:c.1192_1193insG	NP_001160022.1:p.Met398SerfsTer11