Canonical Allele Identifier: CA1672406169

Gene: IYD

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398972T= , CM000668.2:g.150398972T=	GRCh38
NC_000006.11:g.150720108T= , CM000668.1:g.150720108T=	GRCh37
NC_000006.10:g.150761801T=	NCBI36
NG_016007.1:g.35081T=
NG_016007.2:g.35081T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*735T= MANE Select	ENSP00000343763.4:n.*735T=
ENST00000229447.9:c.*835T=	ENSP00000229447.5:n.*835T=
ENST00000344419.7:c.*735T=	ENSP00000343763.3:n.*735T=
NM_001164694.1:c.*835T=	NP_001158166.1:n.*835T=
NM_001164695.1:c.*922T=	NP_001158167.1:n.*922T=
NM_203395.2:c.*735T=	NP_981932.1:n.*735T=
NM_001318495.1:c.*735T=	NP_001305424.1:n.*735T=
NR_134655.1:n.1918T=
NM_001164694.2:c.*835T=	NP_001158166.1:n.*835T=
NM_001164695.2:c.*922T=	NP_001158167.1:n.*922T=
NM_001318495.2:c.*735T=	NP_001305424.1:n.*735T=
NM_203395.3:c.*735T= MANE Select	NP_981932.1:n.*735T=
NR_134655.2:n.1798T=