Canonical Allele Identifier: CA1672401683
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150389486_150389489delinsTTCA , CM000668.2:g.150389486_150389489delinsTTCA GRCh38
NC_000006.11:g.150710622_150710625delinsTTCA , CM000668.1:g.150710622_150710625delinsTTCA GRCh37
NC_000006.10:g.150752315_150752318delinsTTCA NCBI36
NG_016007.1:g.25595_25598delinsTTCA
NG_016007.2:g.25595_25598delinsTTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.313_316delinsTTCA MANE Select ENSP00000343763.4:p.Phe105=
ENST00000229447.9:c.313_316delinsTTCA ENSP00000229447.5:p.Phe105=
ENST00000344419.7:c.313_316delinsTTCA ENSP00000343763.3:p.Phe105=
ENST00000367335.7:c.313_316delinsTTCA ENSP00000356304.3:p.Phe105=
ENST00000392255.7:c.313_316delinsTTCA ENSP00000376084.3:p.Phe105=
ENST00000392256.6:c.313_316delinsTTCA ENSP00000376085.2:p.Phe105=
ENST00000422583.2:c.179+11_179+14delinsTTCA ENSP00000397342.2:n.179+11_179+14delinsTTCA
ENST00000425615.3:c.148_151delinsTTCA ENSP00000390081.3:p.Phe50=
ENST00000500320.7:c.313_316delinsTTCA ENSP00000441276.1:p.Phe105=
ENST00000546121.1:n.256_259delinsTTCA
NM_001164694.1:c.313_316delinsTTCA NP_001158166.1:p.Phe105=
NM_001164695.1:c.313_316delinsTTCA NP_001158167.1:p.Phe105=
NM_203395.2:c.313_316delinsTTCA NP_981932.1:p.Phe105=
XM_006715478.2:c.313_316delinsTTCA XP_006715541.1:p.Phe105=
XM_006715479.2:c.148_151delinsTTCA XP_006715542.1:p.Phe50=
XR_245516.3:n.476_479delinsTTCA
NM_001318495.1:c.124+11_124+14delinsTTCA NP_001305424.1:n.124+11_124+14delinsTTCA
NR_134655.1:n.453_456delinsTTCA
XM_006715478.3:c.313_316delinsTTCA XP_006715541.1:p.Phe105=
XM_006715479.3:c.148_151delinsTTCA XP_006715542.1:p.Phe50=
NM_001164694.2:c.313_316delinsTTCA NP_001158166.1:p.Phe105=
NM_001164695.2:c.313_316delinsTTCA NP_001158167.1:p.Phe105=
NM_001318495.2:c.124+11_124+14delinsTTCA NP_001305424.1:n.124+11_124+14delinsTTCA
NM_203395.3:c.313_316delinsTTCA MANE Select NP_981932.1:p.Phe105=
NR_134655.2:n.333_336delinsTTCA