Canonical Allele Identifier: CA1672406209

Gene: IYD

Linked Data

• dbSNP Id: rs1778427965

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150399050_150399051insG , CM000668.2:g.150399050_150399051insG	GRCh38
NC_000006.11:g.150720186_150720187insG , CM000668.1:g.150720186_150720187insG	GRCh37
NC_000006.10:g.150761879_150761880insG	NCBI36
NG_016007.1:g.35159_35160insG
NG_016007.2:g.35159_35160insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*813_*814insG MANE Select	ENSP00000343763.4:n.*813_*814insG
ENST00000229447.9:c.*913_*914insG	ENSP00000229447.5:n.*913_*914insG
ENST00000344419.7:c.*813_*814insG	ENSP00000343763.3:n.*813_*814insG
NM_001164694.1:c.*913_*914insG	NP_001158166.1:n.*913_*914insG
NM_001164695.1:c.*1000_*1001insG	NP_001158167.1:n.*1000_*1001insG
NM_203395.2:c.*813_*814insG	NP_981932.1:n.*813_*814insG
NM_001318495.1:c.*813_*814insG	NP_001305424.1:n.*813_*814insG
NR_134655.1:n.1996_1997insG
NM_001164694.2:c.*913_*914insG	NP_001158166.1:n.*913_*914insG
NM_001164695.2:c.*1000_*1001insG	NP_001158167.1:n.*1000_*1001insG
NM_001318495.2:c.*813_*814insG	NP_001305424.1:n.*813_*814insG
NM_203395.3:c.*813_*814insG MANE Select	NP_981932.1:n.*813_*814insG
NR_134655.2:n.1876_1877insG