Canonical Allele Identifier: CA366030847
Gene: IYD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150389534A>G , CM000668.2:g.150389534A>G GRCh38
NC_000006.11:g.150710670A>G , CM000668.1:g.150710670A>G GRCh37
NC_000006.10:g.150752363A>G NCBI36
NG_016007.1:g.25643A>G
NG_016007.2:g.25643A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000344419.8:c.361A>G MANE Select ENSP00000343763.4:p.Arg121Gly
ENST00000229447.9:c.361A>G ENSP00000229447.5:p.Arg121Gly
ENST00000344419.7:c.361A>G ENSP00000343763.3:p.Arg121Gly
ENST00000367335.7:c.361A>G ENSP00000356304.3:p.Arg121Gly
ENST00000392255.7:c.361A>G ENSP00000376084.3:p.Arg121Gly
ENST00000392256.6:c.361A>G ENSP00000376085.2:p.Arg121Gly
ENST00000422583.2:c.179+59A>G ENSP00000397342.2:n.179+59A>G
ENST00000425615.3:c.196A>G ENSP00000390081.3:p.Arg66Gly
ENST00000500320.7:c.361A>G ENSP00000441276.1:p.Arg121Gly
ENST00000546121.1:n.304A>G
NM_001164694.1:c.361A>G NP_001158166.1:p.Arg121Gly
NM_001164695.1:c.361A>G NP_001158167.1:p.Arg121Gly
NM_203395.2:c.361A>G NP_981932.1:p.Arg121Gly
XM_006715478.2:c.361A>G XP_006715541.1:p.Arg121Gly
XM_006715479.2:c.196A>G XP_006715542.1:p.Arg66Gly
XR_245516.3:n.524A>G
NM_001318495.1:c.124+59A>G NP_001305424.1:n.124+59A>G
NR_134655.1:n.501A>G
XM_006715478.3:c.361A>G XP_006715541.1:p.Arg121Gly
XM_006715479.3:c.196A>G XP_006715542.1:p.Arg66Gly
NM_001164694.2:c.361A>G NP_001158166.1:p.Arg121Gly
NM_001164695.2:c.361A>G NP_001158167.1:p.Arg121Gly
NM_001318495.2:c.124+59A>G NP_001305424.1:n.124+59A>G
NM_203395.3:c.361A>G MANE Select NP_981932.1:p.Arg121Gly
NR_134655.2:n.381A>G