Canonical Allele Identifier: CA354142166
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993250T>A , CM000665.2:g.121993250T>A GRCh38
NC_000003.11:g.121712097T>A , CM000665.1:g.121712097T>A GRCh37
NC_000003.10:g.123194787T>A NCBI36
NG_031870.1:g.34031A>T
NG_031870.2:g.72305A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1499A>T MANE Select ENSP00000345667.5:p.His500Leu
ENST00000460554.2:n.1449A>T
ENST00000642615.1:c.*682A>T ENSP00000495499.1:n.*682A>T
ENST00000273691.7:c.1367A>T ENSP00000273691.3:p.His456Leu
ENST00000344209.9:c.1499A>T ENSP00000345667.5:p.His500Leu
ENST00000393631.5:c.1232A>T ENSP00000377251.1:p.His411Leu
ENST00000460554.1:n.1601A>T
ENST00000462014.1:c.1403A>T ENSP00000419414.1:p.His468Leu
NM_001199799.1:c.1499A>T NP_001186728.1:p.His500Leu
NM_001199800.1:c.1232A>T NP_001186729.1:p.His411Leu
NM_175924.3:c.1367A>T NP_787120.1:p.His456Leu
XM_005247389.3:c.1403A>T XP_005247446.1:p.His468Leu
XM_011512738.1:c.1499A>T XP_011511040.1:p.His500Leu
XM_011512739.1:c.962A>T XP_011511041.1:p.His321Leu
XM_005247389.4:c.1403A>T XP_005247446.1:p.His468Leu
XM_011512738.2:c.1499A>T XP_011511040.1:p.His500Leu
XM_011512739.2:c.962A>T XP_011511041.1:p.His321Leu
NM_001199799.2:c.1499A>T MANE Select NP_001186728.1:p.His500Leu
NM_001199800.2:c.1232A>T NP_001186729.1:p.His411Leu
NM_175924.4:c.1367A>T NP_787120.1:p.His456Leu