Canonical Allele Identifier: CA354143321
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993524T>G , CM000665.2:g.121993524T>G GRCh38
NC_000003.11:g.121712371T>G , CM000665.1:g.121712371T>G GRCh37
NC_000003.10:g.123195061T>G NCBI36
NG_031870.1:g.33757A>C
NG_031870.2:g.72031A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1225A>C MANE Select ENSP00000345667.5:p.Asn409His
ENST00000460554.2:n.1175A>C
ENST00000642615.1:c.*408A>C ENSP00000495499.1:n.*408A>C
ENST00000273691.7:c.1093A>C ENSP00000273691.3:p.Asn365His
ENST00000344209.9:c.1225A>C ENSP00000345667.5:p.Asn409His
ENST00000393631.5:c.958A>C ENSP00000377251.1:p.Asn320His
ENST00000460554.1:n.1327A>C
ENST00000462014.1:c.1129A>C ENSP00000419414.1:p.Asn377His
NM_001199799.1:c.1225A>C NP_001186728.1:p.Asn409His
NM_001199800.1:c.958A>C NP_001186729.1:p.Asn320His
NM_175924.3:c.1093A>C NP_787120.1:p.Asn365His
XM_005247389.3:c.1129A>C XP_005247446.1:p.Asn377His
XM_011512738.1:c.1225A>C XP_011511040.1:p.Asn409His
XM_011512739.1:c.688A>C XP_011511041.1:p.Asn230His
XM_005247389.4:c.1129A>C XP_005247446.1:p.Asn377His
XM_011512738.2:c.1225A>C XP_011511040.1:p.Asn409His
XM_011512739.2:c.688A>C XP_011511041.1:p.Asn230His
NM_001199799.2:c.1225A>C MANE Select NP_001186728.1:p.Asn409His
NM_001199800.2:c.958A>C NP_001186729.1:p.Asn320His
NM_175924.4:c.1093A>C NP_787120.1:p.Asn365His