Canonical Allele Identifier: CA2568679
Gene: ILDR1 HGNC NCBI

Linked Data

dbSNP Id: rs756778818

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993348G>T , CM000665.2:g.121993348G>T GRCh38
NC_000003.11:g.121712195G>T , CM000665.1:g.121712195G>T GRCh37
NC_000003.10:g.123194885G>T NCBI36
NG_031870.1:g.33933C>A
NG_031870.2:g.72207C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1401C>A MANE Select ENSP00000345667.5:p.Ser467Arg
ENST00000460554.2:n.1351C>A
ENST00000642615.1:c.*584C>A ENSP00000495499.1:n.*584C>A
ENST00000273691.7:c.1269C>A ENSP00000273691.3:p.Ser423Arg
ENST00000344209.9:c.1401C>A ENSP00000345667.5:p.Ser467Arg
ENST00000393631.5:c.1134C>A ENSP00000377251.1:p.Ser378Arg
ENST00000460554.1:n.1503C>A
ENST00000462014.1:c.1305C>A ENSP00000419414.1:p.Ser435Arg
NM_001199799.1:c.1401C>A NP_001186728.1:p.Ser467Arg
NM_001199800.1:c.1134C>A NP_001186729.1:p.Ser378Arg
NM_175924.3:c.1269C>A NP_787120.1:p.Ser423Arg
XM_005247389.3:c.1305C>A XP_005247446.1:p.Ser435Arg
XM_011512738.1:c.1401C>A XP_011511040.1:p.Ser467Arg
XM_011512739.1:c.864C>A XP_011511041.1:p.Ser288Arg
XM_005247389.4:c.1305C>A XP_005247446.1:p.Ser435Arg
XM_011512738.2:c.1401C>A XP_011511040.1:p.Ser467Arg
XM_011512739.2:c.864C>A XP_011511041.1:p.Ser288Arg
NM_001199799.2:c.1401C>A MANE Select NP_001186728.1:p.Ser467Arg
NM_001199800.2:c.1134C>A NP_001186729.1:p.Ser378Arg
NM_175924.4:c.1269C>A NP_787120.1:p.Ser423Arg