Canonical Allele Identifier: CA354144051
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993716T>C , CM000665.2:g.121993716T>C GRCh38
NC_000003.11:g.121712563T>C , CM000665.1:g.121712563T>C GRCh37
NC_000003.10:g.123195253T>C NCBI36
NG_031870.1:g.33565A>G
NG_031870.2:g.71839A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1033A>G MANE Select ENSP00000345667.5:p.Thr345Ala
ENST00000460554.2:n.983A>G
ENST00000642615.1:c.*216A>G ENSP00000495499.1:n.*216A>G
ENST00000273691.7:c.901A>G ENSP00000273691.3:p.Thr301Ala
ENST00000344209.9:c.1033A>G ENSP00000345667.5:p.Thr345Ala
ENST00000393631.5:c.766A>G ENSP00000377251.1:p.Thr256Ala
ENST00000460554.1:n.1135A>G
ENST00000462014.1:c.937A>G ENSP00000419414.1:p.Thr313Ala
NM_001199799.1:c.1033A>G NP_001186728.1:p.Thr345Ala
NM_001199800.1:c.766A>G NP_001186729.1:p.Thr256Ala
NM_175924.3:c.901A>G NP_787120.1:p.Thr301Ala
XM_005247389.3:c.937A>G XP_005247446.1:p.Thr313Ala
XM_011512738.1:c.1033A>G XP_011511040.1:p.Thr345Ala
XM_011512739.1:c.496A>G XP_011511041.1:p.Thr166Ala
XM_005247389.4:c.937A>G XP_005247446.1:p.Thr313Ala
XM_011512738.2:c.1033A>G XP_011511040.1:p.Thr345Ala
XM_011512739.2:c.496A>G XP_011511041.1:p.Thr166Ala
NM_001199799.2:c.1033A>G MANE Select NP_001186728.1:p.Thr345Ala
NM_001199800.2:c.766A>G NP_001186729.1:p.Thr256Ala
NM_175924.4:c.901A>G NP_787120.1:p.Thr301Ala