Canonical Allele Identifier: CA366030278

Gene: IYD

Linked Data

• MyVariant Identifiers: chr6:g.150710575G>C (hg19) ; chr6:g.150389439G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.150389439G>C , CM000668.2:g.150389439G>C	GRCh38
NC_000006.11:g.150710575G>C , CM000668.1:g.150710575G>C	GRCh37
NC_000006.10:g.150752268G>C	NCBI36
NG_016007.1:g.25548G>C
NG_016007.2:g.25548G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000344419.8:c.266G>C MANE Select	ENSP00000343763.4:p.Arg89Thr
ENST00000229447.9:c.266G>C	ENSP00000229447.5:p.Arg89Thr
ENST00000344419.7:c.266G>C	ENSP00000343763.3:p.Arg89Thr
ENST00000367335.7:c.266G>C	ENSP00000356304.3:p.Arg89Thr
ENST00000392255.7:c.266G>C	ENSP00000376084.3:p.Arg89Thr
ENST00000392256.6:c.266G>C	ENSP00000376085.2:p.Arg89Thr
ENST00000422583.2:c.143G>C	ENSP00000397342.2:p.Arg48Thr
ENST00000425615.3:c.101G>C	ENSP00000390081.3:p.Arg34Thr
ENST00000500320.7:c.266G>C	ENSP00000441276.1:p.Arg89Thr
ENST00000546121.1:n.209G>C
NM_001164694.1:c.266G>C	NP_001158166.1:p.Arg89Thr
NM_001164695.1:c.266G>C	NP_001158167.1:p.Arg89Thr
NM_203395.2:c.266G>C	NP_981932.1:p.Arg89Thr
XM_006715478.2:c.266G>C	XP_006715541.1:p.Arg89Thr
XM_006715479.2:c.101G>C	XP_006715542.1:p.Arg34Thr
XR_245516.3:n.429G>C
NM_001318495.1:c.88G>C	NP_001305424.1:p.Gly30Arg
NR_134655.1:n.406G>C
XM_006715478.3:c.266G>C	XP_006715541.1:p.Arg89Thr
XM_006715479.3:c.101G>C	XP_006715542.1:p.Arg34Thr
NM_001164694.2:c.266G>C	NP_001158166.1:p.Arg89Thr
NM_001164695.2:c.266G>C	NP_001158167.1:p.Arg89Thr
NM_001318495.2:c.88G>C	NP_001305424.1:p.Gly30Arg
NM_203395.3:c.266G>C MANE Select	NP_981932.1:p.Arg89Thr
NR_134655.2:n.286G>C