Canonical Allele Identifier: CA354143386
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993545T>C , CM000665.2:g.121993545T>C GRCh38
NC_000003.11:g.121712392T>C , CM000665.1:g.121712392T>C GRCh37
NC_000003.10:g.123195082T>C NCBI36
NG_031870.1:g.33736A>G
NG_031870.2:g.72010A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1204A>G MANE Select ENSP00000345667.5:p.Arg402Gly
ENST00000460554.2:n.1154A>G
ENST00000642615.1:c.*387A>G ENSP00000495499.1:n.*387A>G
ENST00000273691.7:c.1072A>G ENSP00000273691.3:p.Arg358Gly
ENST00000344209.9:c.1204A>G ENSP00000345667.5:p.Arg402Gly
ENST00000393631.5:c.937A>G ENSP00000377251.1:p.Arg313Gly
ENST00000460554.1:n.1306A>G
ENST00000462014.1:c.1108A>G ENSP00000419414.1:p.Arg370Gly
NM_001199799.1:c.1204A>G NP_001186728.1:p.Arg402Gly
NM_001199800.1:c.937A>G NP_001186729.1:p.Arg313Gly
NM_175924.3:c.1072A>G NP_787120.1:p.Arg358Gly
XM_005247389.3:c.1108A>G XP_005247446.1:p.Arg370Gly
XM_011512738.1:c.1204A>G XP_011511040.1:p.Arg402Gly
XM_011512739.1:c.667A>G XP_011511041.1:p.Arg223Gly
XM_005247389.4:c.1108A>G XP_005247446.1:p.Arg370Gly
XM_011512738.2:c.1204A>G XP_011511040.1:p.Arg402Gly
XM_011512739.2:c.667A>G XP_011511041.1:p.Arg223Gly
NM_001199799.2:c.1204A>G MANE Select NP_001186728.1:p.Arg402Gly
NM_001199800.2:c.937A>G NP_001186729.1:p.Arg313Gly
NM_175924.4:c.1072A>G NP_787120.1:p.Arg358Gly