Canonical Allele Identifier: CA1672406079

Gene: IYD

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398790C= , CM000668.2:g.150398790C=	GRCh38
NC_000006.11:g.150719926C= , CM000668.1:g.150719926C=	GRCh37
NC_000006.10:g.150761619C=	NCBI36
NG_016007.1:g.34899C=
NG_016007.2:g.34899C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*553C= MANE Select	ENSP00000343763.4:n.*553C=
ENST00000229447.9:c.*653C=	ENSP00000229447.5:n.*653C=
ENST00000344419.7:c.*553C=	ENSP00000343763.3:n.*553C=
NM_001164694.1:c.*653C=	NP_001158166.1:n.*653C=
NM_001164695.1:c.*740C=	NP_001158167.1:n.*740C=
NM_203395.2:c.*553C=	NP_981932.1:n.*553C=
NM_001318495.1:c.*553C=	NP_001305424.1:n.*553C=
NR_134655.1:n.1736C=
NM_001164694.2:c.*653C=	NP_001158166.1:n.*653C=
NM_001164695.2:c.*740C=	NP_001158167.1:n.*740C=
NM_001318495.2:c.*553C=	NP_001305424.1:n.*553C=
NM_203395.3:c.*553C= MANE Select	NP_981932.1:n.*553C=
NR_134655.2:n.1616C=