Canonical Allele Identifier: CA1672401634

Gene: IYD

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150389365G= , CM000668.2:g.150389365G=	GRCh38
NC_000006.11:g.150710501G= , CM000668.1:g.150710501G=	GRCh37
NC_000006.10:g.150752194G=	NCBI36
NG_016007.1:g.25474G=
NG_016007.2:g.25474G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.192G= MANE Select	ENSP00000343763.4:p.Trp64=
ENST00000229447.9:c.192G=	ENSP00000229447.5:p.Trp64=
ENST00000344419.7:c.192G=	ENSP00000343763.3:p.Trp64=
ENST00000367335.7:c.192G=	ENSP00000356304.3:p.Trp64=
ENST00000392255.7:c.192G=	ENSP00000376084.3:p.Trp64=
ENST00000392256.6:c.192G=	ENSP00000376085.2:p.Trp64=
ENST00000422583.2:c.69G=	ENSP00000397342.2:p.Trp23=
ENST00000425615.3:c.27G=	ENSP00000390081.3:p.Trp9=
ENST00000500320.7:c.192G=	ENSP00000441276.1:p.Trp64=
ENST00000546121.1:n.135G=
NM_001164694.1:c.192G=	NP_001158166.1:p.Trp64=
NM_001164695.1:c.192G=	NP_001158167.1:p.Trp64=
NM_203395.2:c.192G=	NP_981932.1:p.Trp64=
XM_006715478.2:c.192G=	XP_006715541.1:p.Trp64=
XM_006715479.2:c.27G=	XP_006715542.1:p.Trp9=
XR_245516.3:n.355G=
NM_001318495.1:c.14G=	NP_001305424.1:p.Gly5=
NR_134655.1:n.332G=
XM_006715478.3:c.192G=	XP_006715541.1:p.Trp64=
XM_006715479.3:c.27G=	XP_006715542.1:p.Trp9=
NM_001164694.2:c.192G=	NP_001158166.1:p.Trp64=
NM_001164695.2:c.192G=	NP_001158167.1:p.Trp64=
NM_001318495.2:c.14G=	NP_001305424.1:p.Gly5=
NM_203395.3:c.192G= MANE Select	NP_981932.1:p.Trp64=
NR_134655.2:n.212G=