Canonical Allele Identifier: CA1672406052

Gene: IYD

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150398726T= , CM000668.2:g.150398726T=	GRCh38
NC_000006.11:g.150719862T= , CM000668.1:g.150719862T=	GRCh37
NC_000006.10:g.150761555T=	NCBI36
NG_016007.1:g.34835T=
NG_016007.2:g.34835T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*489T= MANE Select	ENSP00000343763.4:n.*489T=
ENST00000229447.9:c.*589T=	ENSP00000229447.5:n.*589T=
ENST00000344419.7:c.*489T=	ENSP00000343763.3:n.*489T=
NM_001164694.1:c.*589T=	NP_001158166.1:n.*589T=
NM_001164695.1:c.*676T=	NP_001158167.1:n.*676T=
NM_203395.2:c.*489T=	NP_981932.1:n.*489T=
NM_001318495.1:c.*489T=	NP_001305424.1:n.*489T=
NR_134655.1:n.1672T=
NM_001164694.2:c.*589T=	NP_001158166.1:n.*589T=
NM_001164695.2:c.*676T=	NP_001158167.1:n.*676T=
NM_001318495.2:c.*489T=	NP_001305424.1:n.*489T=
NM_203395.3:c.*489T= MANE Select	NP_981932.1:n.*489T=
NR_134655.2:n.1552T=