Canonical Allele Identifier: CA366030391
Gene: IYD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150389455T>G , CM000668.2:g.150389455T>G GRCh38
NC_000006.11:g.150710591T>G , CM000668.1:g.150710591T>G GRCh37
NC_000006.10:g.150752284T>G NCBI36
NG_016007.1:g.25564T>G
NG_016007.2:g.25564T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.282T>G MANE Select ENSP00000343763.4:p.Tyr94Ter
ENST00000229447.9:c.282T>G ENSP00000229447.5:p.Tyr94Ter
ENST00000344419.7:c.282T>G ENSP00000343763.3:p.Tyr94Ter
ENST00000367335.7:c.282T>G ENSP00000356304.3:p.Tyr94Ter
ENST00000392255.7:c.282T>G ENSP00000376084.3:p.Tyr94Ter
ENST00000392256.6:c.282T>G ENSP00000376085.2:p.Tyr94Ter
ENST00000422583.2:c.159T>G ENSP00000397342.2:p.Tyr53Ter
ENST00000425615.3:c.117T>G ENSP00000390081.3:p.Tyr39Ter
ENST00000500320.7:c.282T>G ENSP00000441276.1:p.Tyr94Ter
ENST00000546121.1:n.225T>G
NM_001164694.1:c.282T>G NP_001158166.1:p.Tyr94Ter
NM_001164695.1:c.282T>G NP_001158167.1:p.Tyr94Ter
NM_203395.2:c.282T>G NP_981932.1:p.Tyr94Ter
XM_006715478.2:c.282T>G XP_006715541.1:p.Tyr94Ter
XM_006715479.2:c.117T>G XP_006715542.1:p.Tyr39Ter
XR_245516.3:n.445T>G
NM_001318495.1:c.104T>G NP_001305424.1:p.Met35Arg
NR_134655.1:n.422T>G
XM_006715478.3:c.282T>G XP_006715541.1:p.Tyr94Ter
XM_006715479.3:c.117T>G XP_006715542.1:p.Tyr39Ter
NM_001164694.2:c.282T>G NP_001158166.1:p.Tyr94Ter
NM_001164695.2:c.282T>G NP_001158167.1:p.Tyr94Ter
NM_001318495.2:c.104T>G NP_001305424.1:p.Met35Arg
NM_203395.3:c.282T>G MANE Select NP_981932.1:p.Tyr94Ter
NR_134655.2:n.302T>G