Canonical Allele Identifier: CA651454641

Gene: IYD

Linked Data

• COSMIC: COSN14704150

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398581_150398582insT , CM000668.2:g.150398581_150398582insT	GRCh38
NC_000006.11:g.150719717_150719718insT , CM000668.1:g.150719717_150719718insT	GRCh37
NC_000006.10:g.150761410_150761411insT	NCBI36
NG_016007.1:g.34690_34691insT
NG_016007.2:g.34690_34691insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*344_*345insT MANE Select	ENSP00000343763.4:n.*344_*345insT
ENST00000229447.9:c.*444_*445insT	ENSP00000229447.5:n.*444_*445insT
ENST00000344419.7:c.*344_*345insT	ENSP00000343763.3:n.*344_*345insT
NM_001164694.1:c.*444_*445insT	NP_001158166.1:n.*444_*445insT
NM_001164695.1:c.*531_*532insT	NP_001158167.1:n.*531_*532insT
NM_203395.2:c.*344_*345insT	NP_981932.1:n.*344_*345insT
NM_001318495.1:c.*344_*345insT	NP_001305424.1:n.*344_*345insT
NR_134655.1:n.1527_1528insT
NM_001164694.2:c.*444_*445insT	NP_001158166.1:n.*444_*445insT
NM_001164695.2:c.*531_*532insT	NP_001158167.1:n.*531_*532insT
NM_001318495.2:c.*344_*345insT	NP_001305424.1:n.*344_*345insT
NM_203395.3:c.*344_*345insT MANE Select	NP_981932.1:n.*344_*345insT
NR_134655.2:n.1407_1408insT