Canonical Allele Identifier: CA1672406013

Gene: IYD

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398642T= , CM000668.2:g.150398642T=	GRCh38
NC_000006.11:g.150719778T= , CM000668.1:g.150719778T=	GRCh37
NC_000006.10:g.150761471T=	NCBI36
NG_016007.1:g.34751T=
NG_016007.2:g.34751T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*405T= MANE Select	ENSP00000343763.4:n.*405T=
ENST00000229447.9:c.*505T=	ENSP00000229447.5:n.*505T=
ENST00000344419.7:c.*405T=	ENSP00000343763.3:n.*405T=
NM_001164694.1:c.*505T=	NP_001158166.1:n.*505T=
NM_001164695.1:c.*592T=	NP_001158167.1:n.*592T=
NM_203395.2:c.*405T=	NP_981932.1:n.*405T=
NM_001318495.1:c.*405T=	NP_001305424.1:n.*405T=
NR_134655.1:n.1588T=
NM_001164694.2:c.*505T=	NP_001158166.1:n.*505T=
NM_001164695.2:c.*592T=	NP_001158167.1:n.*592T=
NM_001318495.2:c.*405T=	NP_001305424.1:n.*405T=
NM_203395.3:c.*405T= MANE Select	NP_981932.1:n.*405T=
NR_134655.2:n.1468T=