Canonical Allele Identifier: CA354143377
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993542G>T , CM000665.2:g.121993542G>T GRCh38
NC_000003.11:g.121712389G>T , CM000665.1:g.121712389G>T GRCh37
NC_000003.10:g.123195079G>T NCBI36
NG_031870.1:g.33739C>A
NG_031870.2:g.72013C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1207C>A MANE Select ENSP00000345667.5:p.His403Asn
ENST00000460554.2:n.1157C>A
ENST00000642615.1:c.*390C>A ENSP00000495499.1:n.*390C>A
ENST00000273691.7:c.1075C>A ENSP00000273691.3:p.His359Asn
ENST00000344209.9:c.1207C>A ENSP00000345667.5:p.His403Asn
ENST00000393631.5:c.940C>A ENSP00000377251.1:p.His314Asn
ENST00000460554.1:n.1309C>A
ENST00000462014.1:c.1111C>A ENSP00000419414.1:p.His371Asn
NM_001199799.1:c.1207C>A NP_001186728.1:p.His403Asn
NM_001199800.1:c.940C>A NP_001186729.1:p.His314Asn
NM_175924.3:c.1075C>A NP_787120.1:p.His359Asn
XM_005247389.3:c.1111C>A XP_005247446.1:p.His371Asn
XM_011512738.1:c.1207C>A XP_011511040.1:p.His403Asn
XM_011512739.1:c.670C>A XP_011511041.1:p.His224Asn
XM_005247389.4:c.1111C>A XP_005247446.1:p.His371Asn
XM_011512738.2:c.1207C>A XP_011511040.1:p.His403Asn
XM_011512739.2:c.670C>A XP_011511041.1:p.His224Asn
NM_001199799.2:c.1207C>A MANE Select NP_001186728.1:p.His403Asn
NM_001199800.2:c.940C>A NP_001186729.1:p.His314Asn
NM_175924.4:c.1075C>A NP_787120.1:p.His359Asn