Canonical Allele Identifier: CA1672401667

Gene: IYD

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150389440G= , CM000668.2:g.150389440G=	GRCh38
NC_000006.11:g.150710576G= , CM000668.1:g.150710576G=	GRCh37
NC_000006.10:g.150752269G=	NCBI36
NG_016007.1:g.25549G=
NG_016007.2:g.25549G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000344419.8:c.267G= MANE Select	ENSP00000343763.4:p.Arg89=
ENST00000229447.9:c.267G=	ENSP00000229447.5:p.Arg89=
ENST00000344419.7:c.267G=	ENSP00000343763.3:p.Arg89=
ENST00000367335.7:c.267G=	ENSP00000356304.3:p.Arg89=
ENST00000392255.7:c.267G=	ENSP00000376084.3:p.Arg89=
ENST00000392256.6:c.267G=	ENSP00000376085.2:p.Arg89=
ENST00000422583.2:c.144G=	ENSP00000397342.2:p.Arg48=
ENST00000425615.3:c.102G=	ENSP00000390081.3:p.Arg34=
ENST00000500320.7:c.267G=	ENSP00000441276.1:p.Arg89=
ENST00000546121.1:n.210G=
NM_001164694.1:c.267G=	NP_001158166.1:p.Arg89=
NM_001164695.1:c.267G=	NP_001158167.1:p.Arg89=
NM_203395.2:c.267G=	NP_981932.1:p.Arg89=
XM_006715478.2:c.267G=	XP_006715541.1:p.Arg89=
XM_006715479.2:c.102G=	XP_006715542.1:p.Arg34=
XR_245516.3:n.430G=
NM_001318495.1:c.89G=	NP_001305424.1:p.Gly30=
NR_134655.1:n.407G=
XM_006715478.3:c.267G=	XP_006715541.1:p.Arg89=
XM_006715479.3:c.102G=	XP_006715542.1:p.Arg34=
NM_001164694.2:c.267G=	NP_001158166.1:p.Arg89=
NM_001164695.2:c.267G=	NP_001158167.1:p.Arg89=
NM_001318495.2:c.89G=	NP_001305424.1:p.Gly30=
NM_203395.3:c.267G= MANE Select	NP_981932.1:p.Arg89=
NR_134655.2:n.287G=