Canonical Allele Identifier: CA1095800239

Gene: IYD

Linked Data

• gnomAD v3: 6-150398702-A-ATTTT
• gnomAD v4: 6-150398702-A-ATTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398702_150398703insTTTT , CM000668.2:g.150398702_150398703insTTTT	GRCh38
NC_000006.11:g.150719838_150719839insTTTT , CM000668.1:g.150719838_150719839insTTTT	GRCh37
NC_000006.10:g.150761531_150761532insTTTT	NCBI36
NG_016007.1:g.34811_34812insTTTT
NG_016007.2:g.34811_34812insTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*465_*466insTTTT MANE Select	ENSP00000343763.4:n.*465_*466insTTTT
ENST00000229447.9:c.*565_*566insTTTT	ENSP00000229447.5:n.*565_*566insTTTT
ENST00000344419.7:c.*465_*466insTTTT	ENSP00000343763.3:n.*465_*466insTTTT
NM_001164694.1:c.*565_*566insTTTT	NP_001158166.1:n.*565_*566insTTTT
NM_001164695.1:c.*652_*653insTTTT	NP_001158167.1:n.*652_*653insTTTT
NM_203395.2:c.*465_*466insTTTT	NP_981932.1:n.*465_*466insTTTT
NM_001318495.1:c.*465_*466insTTTT	NP_001305424.1:n.*465_*466insTTTT
NR_134655.1:n.1648_1649insTTTT
NM_001164694.2:c.*565_*566insTTTT	NP_001158166.1:n.*565_*566insTTTT
NM_001164695.2:c.*652_*653insTTTT	NP_001158167.1:n.*652_*653insTTTT
NM_001318495.2:c.*465_*466insTTTT	NP_001305424.1:n.*465_*466insTTTT
NM_203395.3:c.*465_*466insTTTT MANE Select	NP_981932.1:n.*465_*466insTTTT
NR_134655.2:n.1528_1529insTTTT