Canonical Allele Identifier: CA1672406196

Gene: IYD

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150399030G= , CM000668.2:g.150399030G=	GRCh38
NC_000006.11:g.150720166G= , CM000668.1:g.150720166G=	GRCh37
NC_000006.10:g.150761859G=	NCBI36
NG_016007.1:g.35139G=
NG_016007.2:g.35139G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.*793G= MANE Select	ENSP00000343763.4:n.*793G=
ENST00000229447.9:c.*893G=	ENSP00000229447.5:n.*893G=
ENST00000344419.7:c.*793G=	ENSP00000343763.3:n.*793G=
NM_001164694.1:c.*893G=	NP_001158166.1:n.*893G=
NM_001164695.1:c.*980G=	NP_001158167.1:n.*980G=
NM_203395.2:c.*793G=	NP_981932.1:n.*793G=
NM_001318495.1:c.*793G=	NP_001305424.1:n.*793G=
NR_134655.1:n.1976G=
NM_001164694.2:c.*893G=	NP_001158166.1:n.*893G=
NM_001164695.2:c.*980G=	NP_001158167.1:n.*980G=
NM_001318495.2:c.*793G=	NP_001305424.1:n.*793G=
NM_203395.3:c.*793G= MANE Select	NP_981932.1:n.*793G=
NR_134655.2:n.1856G=