Canonical Allele Identifier: CA1672406195

Gene: IYD

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150399029C= , CM000668.2:g.150399029C=	GRCh38
NC_000006.11:g.150720165C= , CM000668.1:g.150720165C=	GRCh37
NC_000006.10:g.150761858C=	NCBI36
NG_016007.1:g.35138C=
NG_016007.2:g.35138C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*792C= MANE Select	ENSP00000343763.4:n.*792C=
ENST00000229447.9:c.*892C=	ENSP00000229447.5:n.*892C=
ENST00000344419.7:c.*792C=	ENSP00000343763.3:n.*792C=
NM_001164694.1:c.*892C=	NP_001158166.1:n.*892C=
NM_001164695.1:c.*979C=	NP_001158167.1:n.*979C=
NM_203395.2:c.*792C=	NP_981932.1:n.*792C=
NM_001318495.1:c.*792C=	NP_001305424.1:n.*792C=
NR_134655.1:n.1975C=
NM_001164694.2:c.*892C=	NP_001158166.1:n.*892C=
NM_001164695.2:c.*979C=	NP_001158167.1:n.*979C=
NM_001318495.2:c.*792C=	NP_001305424.1:n.*792C=
NM_203395.3:c.*792C= MANE Select	NP_981932.1:n.*792C=
NR_134655.2:n.1855C=