Canonical Allele Identifier: CA1672406134

Gene: IYD

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398906_150398911delinsGCACTT , CM000668.2:g.150398906_150398911delinsGCACTT	GRCh38
NC_000006.11:g.150720042_150720047delinsGCACTT , CM000668.1:g.150720042_150720047delinsGCACTT	GRCh37
NC_000006.10:g.150761735_150761740delinsGCACTT	NCBI36
NG_016007.1:g.35015_35020delinsGCACTT
NG_016007.2:g.35015_35020delinsGCACTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*669_*674delinsGCACTT MANE Select	ENSP00000343763.4:n.*669_*674delinsGCACTT
ENST00000229447.9:c.*769_*774delinsGCACTT	ENSP00000229447.5:n.*769_*774delinsGCACTT
ENST00000344419.7:c.*669_*674delinsGCACTT	ENSP00000343763.3:n.*669_*674delinsGCACTT
NM_001164694.1:c.*769_*774delinsGCACTT	NP_001158166.1:n.*769_*774delinsGCACTT
NM_001164695.1:c.*856_*861delinsGCACTT	NP_001158167.1:n.*856_*861delinsGCACTT
NM_203395.2:c.*669_*674delinsGCACTT	NP_981932.1:n.*669_*674delinsGCACTT
NM_001318495.1:c.*669_*674delinsGCACTT	NP_001305424.1:n.*669_*674delinsGCACTT
NR_134655.1:n.1852_1857delinsGCACTT
NM_001164694.2:c.*769_*774delinsGCACTT	NP_001158166.1:n.*769_*774delinsGCACTT
NM_001164695.2:c.*856_*861delinsGCACTT	NP_001158167.1:n.*856_*861delinsGCACTT
NM_001318495.2:c.*669_*674delinsGCACTT	NP_001305424.1:n.*669_*674delinsGCACTT
NM_203395.3:c.*669_*674delinsGCACTT MANE Select	NP_981932.1:n.*669_*674delinsGCACTT
NR_134655.2:n.1732_1737delinsGCACTT