Canonical Allele Identifier: CA1672406178

Gene: IYD

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398991T= , CM000668.2:g.150398991T=	GRCh38
NC_000006.11:g.150720127T= , CM000668.1:g.150720127T=	GRCh37
NC_000006.10:g.150761820T=	NCBI36
NG_016007.1:g.35100T=
NG_016007.2:g.35100T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*754T= MANE Select	ENSP00000343763.4:n.*754T=
ENST00000229447.9:c.*854T=	ENSP00000229447.5:n.*854T=
ENST00000344419.7:c.*754T=	ENSP00000343763.3:n.*754T=
NM_001164694.1:c.*854T=	NP_001158166.1:n.*854T=
NM_001164695.1:c.*941T=	NP_001158167.1:n.*941T=
NM_203395.2:c.*754T=	NP_981932.1:n.*754T=
NM_001318495.1:c.*754T=	NP_001305424.1:n.*754T=
NR_134655.1:n.1937T=
NM_001164694.2:c.*854T=	NP_001158166.1:n.*854T=
NM_001164695.2:c.*941T=	NP_001158167.1:n.*941T=
NM_001318495.2:c.*754T=	NP_001305424.1:n.*754T=
NM_203395.3:c.*754T= MANE Select	NP_981932.1:n.*754T=
NR_134655.2:n.1817T=