Canonical Allele Identifier: CA1672401629

Gene: IYD

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150389357G= , CM000668.2:g.150389357G=	GRCh38
NC_000006.11:g.150710493G= , CM000668.1:g.150710493G=	GRCh37
NC_000006.10:g.150752186G=	NCBI36
NG_016007.1:g.25466G=
NG_016007.2:g.25466G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.184G= MANE Select	ENSP00000343763.4:p.Asp62=
ENST00000229447.9:c.184G=	ENSP00000229447.5:p.Asp62=
ENST00000344419.7:c.184G=	ENSP00000343763.3:p.Asp62=
ENST00000367335.7:c.184G=	ENSP00000356304.3:p.Asp62=
ENST00000392255.7:c.184G=	ENSP00000376084.3:p.Asp62=
ENST00000392256.6:c.184G=	ENSP00000376085.2:p.Asp62=
ENST00000422583.2:c.61G=	ENSP00000397342.2:p.Asp21=
ENST00000425615.3:c.19G=	ENSP00000390081.3:p.Asp7=
ENST00000500320.7:c.184G=	ENSP00000441276.1:p.Asp62=
ENST00000546121.1:n.127G=
NM_001164694.1:c.184G=	NP_001158166.1:p.Asp62=
NM_001164695.1:c.184G=	NP_001158167.1:p.Asp62=
NM_203395.2:c.184G=	NP_981932.1:p.Asp62=
XM_006715478.2:c.184G=	XP_006715541.1:p.Asp62=
XM_006715479.2:c.19G=	XP_006715542.1:p.Asp7=
XR_245516.3:n.347G=
NM_001318495.1:c.6G=	NP_001305424.1:p.Leu2=
NR_134655.1:n.324G=
XM_006715478.3:c.184G=	XP_006715541.1:p.Asp62=
XM_006715479.3:c.19G=	XP_006715542.1:p.Asp7=
NM_001164694.2:c.184G=	NP_001158166.1:p.Asp62=
NM_001164695.2:c.184G=	NP_001158167.1:p.Asp62=
NM_001318495.2:c.6G=	NP_001305424.1:p.Leu2=
NM_203395.3:c.184G= MANE Select	NP_981932.1:p.Asp62=
NR_134655.2:n.204G=