Canonical Allele Identifier: CA1672401624
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150389329A= , CM000668.2:g.150389329A= GRCh38
NC_000006.11:g.150710465A= , CM000668.1:g.150710465A= GRCh37
NC_000006.10:g.150752158A= NCBI36
NG_016007.1:g.25438A=
NG_016007.2:g.25438A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.179-23A= MANE Select ENSP00000343763.4:n.179-23A=
ENST00000229447.9:c.179-23A= ENSP00000229447.5:n.179-23A=
ENST00000344419.7:c.179-23A= ENSP00000343763.3:n.179-23A=
ENST00000367335.7:c.179-23A= ENSP00000356304.3:n.179-23A=
ENST00000392255.7:c.179-23A= ENSP00000376084.3:n.179-23A=
ENST00000392256.6:c.179-23A= ENSP00000376085.2:n.179-23A=
ENST00000422583.2:c.56-23A= ENSP00000397342.2:n.56-23A=
ENST00000425615.3:c.14-23A= ENSP00000390081.3:n.14-23A=
ENST00000500320.7:c.179-23A= ENSP00000441276.1:n.179-23A=
ENST00000546121.1:n.122-23A=
NM_001164694.1:c.179-23A= NP_001158166.1:n.179-23A=
NM_001164695.1:c.179-23A= NP_001158167.1:n.179-23A=
NM_203395.2:c.179-23A= NP_981932.1:n.179-23A=
XM_006715478.2:c.179-23A= XP_006715541.1:n.179-23A=
XM_006715479.2:c.14-23A= XP_006715542.1:n.14-23A=
XR_245516.3:n.342-23A=
NM_001318495.1:c.1-23A= NP_001305424.1:n.1-23A=
NR_134655.1:n.319-23A=
XM_006715478.3:c.179-23A= XP_006715541.1:n.179-23A=
XM_006715479.3:c.14-23A= XP_006715542.1:n.14-23A=
NM_001164694.2:c.179-23A= NP_001158166.1:n.179-23A=
NM_001164695.2:c.179-23A= NP_001158167.1:n.179-23A=
NM_001318495.2:c.1-23A= NP_001305424.1:n.1-23A=
NM_203395.3:c.179-23A= MANE Select NP_981932.1:n.179-23A=
NR_134655.2:n.199-23A=