Canonical Allele Identifier: CA1672401664

Gene: IYD

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150389434_150389436delinsTAA , CM000668.2:g.150389434_150389436delinsTAA	GRCh38
NC_000006.11:g.150710570_150710572delinsTAA , CM000668.1:g.150710570_150710572delinsTAA	GRCh37
NC_000006.10:g.150752263_150752265delinsTAA	NCBI36
NG_016007.1:g.25543_25545delinsTAA
NG_016007.2:g.25543_25545delinsTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344419.8:c.261_263delinsTAA MANE Select	ENSP00000343763.4:p.Val87=
ENST00000229447.9:c.261_263delinsTAA	ENSP00000229447.5:p.Val87=
ENST00000344419.7:c.261_263delinsTAA	ENSP00000343763.3:p.Val87=
ENST00000367335.7:c.261_263delinsTAA	ENSP00000356304.3:p.Val87=
ENST00000392255.7:c.261_263delinsTAA	ENSP00000376084.3:p.Val87=
ENST00000392256.6:c.261_263delinsTAA	ENSP00000376085.2:p.Val87=
ENST00000422583.2:c.138_140delinsTAA	ENSP00000397342.2:p.Val46=
ENST00000425615.3:c.96_98delinsTAA	ENSP00000390081.3:p.Val32=
ENST00000500320.7:c.261_263delinsTAA	ENSP00000441276.1:p.Val87=
ENST00000546121.1:n.204_206delinsTAA
NM_001164694.1:c.261_263delinsTAA	NP_001158166.1:p.Val87=
NM_001164695.1:c.261_263delinsTAA	NP_001158167.1:p.Val87=
NM_203395.2:c.261_263delinsTAA	NP_981932.1:p.Val87=
XM_006715478.2:c.261_263delinsTAA	XP_006715541.1:p.Val87=
XM_006715479.2:c.96_98delinsTAA	XP_006715542.1:p.Val32=
XR_245516.3:n.424_426delinsTAA
NM_001318495.1:c.83_85delinsTAA	NP_001305424.1:p.Leu28=
NR_134655.1:n.401_403delinsTAA
XM_006715478.3:c.261_263delinsTAA	XP_006715541.1:p.Val87=
XM_006715479.3:c.96_98delinsTAA	XP_006715542.1:p.Val32=
NM_001164694.2:c.261_263delinsTAA	NP_001158166.1:p.Val87=
NM_001164695.2:c.261_263delinsTAA	NP_001158167.1:p.Val87=
NM_001318495.2:c.83_85delinsTAA	NP_001305424.1:p.Leu28=
NM_203395.3:c.261_263delinsTAA MANE Select	NP_981932.1:p.Val87=
NR_134655.2:n.281_283delinsTAA