Canonical Allele Identifier: CA1672401685

Gene: IYD

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150389488C= , CM000668.2:g.150389488C=	GRCh38
NC_000006.11:g.150710624C= , CM000668.1:g.150710624C=	GRCh37
NC_000006.10:g.150752317C=	NCBI36
NG_016007.1:g.25597C=
NG_016007.2:g.25597C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.315C= MANE Select	ENSP00000343763.4:p.Phe105=
ENST00000229447.9:c.315C=	ENSP00000229447.5:p.Phe105=
ENST00000344419.7:c.315C=	ENSP00000343763.3:p.Phe105=
ENST00000367335.7:c.315C=	ENSP00000356304.3:p.Phe105=
ENST00000392255.7:c.315C=	ENSP00000376084.3:p.Phe105=
ENST00000392256.6:c.315C=	ENSP00000376085.2:p.Phe105=
ENST00000422583.2:c.179+13C=	ENSP00000397342.2:n.179+13C=
ENST00000425615.3:c.150C=	ENSP00000390081.3:p.Phe50=
ENST00000500320.7:c.315C=	ENSP00000441276.1:p.Phe105=
ENST00000546121.1:n.258C=
NM_001164694.1:c.315C=	NP_001158166.1:p.Phe105=
NM_001164695.1:c.315C=	NP_001158167.1:p.Phe105=
NM_203395.2:c.315C=	NP_981932.1:p.Phe105=
XM_006715478.2:c.315C=	XP_006715541.1:p.Phe105=
XM_006715479.2:c.150C=	XP_006715542.1:p.Phe50=
XR_245516.3:n.478C=
NM_001318495.1:c.124+13C=	NP_001305424.1:n.124+13C=
NR_134655.1:n.455C=
XM_006715478.3:c.315C=	XP_006715541.1:p.Phe105=
XM_006715479.3:c.150C=	XP_006715542.1:p.Phe50=
NM_001164694.2:c.315C=	NP_001158166.1:p.Phe105=
NM_001164695.2:c.315C=	NP_001158167.1:p.Phe105=
NM_001318495.2:c.124+13C=	NP_001305424.1:n.124+13C=
NM_203395.3:c.315C= MANE Select	NP_981932.1:p.Phe105=
NR_134655.2:n.335C=