Canonical Allele Identifier: CA354143970
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993679A>T , CM000665.2:g.121993679A>T GRCh38
NC_000003.11:g.121712526A>T , CM000665.1:g.121712526A>T GRCh37
NC_000003.10:g.123195216A>T NCBI36
NG_031870.1:g.33602T>A
NG_031870.2:g.71876T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1070T>A MANE Select ENSP00000345667.5:p.Ile357Asn
ENST00000460554.2:n.1020T>A
ENST00000642615.1:c.*253T>A ENSP00000495499.1:n.*253T>A
ENST00000273691.7:c.938T>A ENSP00000273691.3:p.Ile313Asn
ENST00000344209.9:c.1070T>A ENSP00000345667.5:p.Ile357Asn
ENST00000393631.5:c.803T>A ENSP00000377251.1:p.Ile268Asn
ENST00000460554.1:n.1172T>A
ENST00000462014.1:c.974T>A ENSP00000419414.1:p.Ile325Asn
NM_001199799.1:c.1070T>A NP_001186728.1:p.Ile357Asn
NM_001199800.1:c.803T>A NP_001186729.1:p.Ile268Asn
NM_175924.3:c.938T>A NP_787120.1:p.Ile313Asn
XM_005247389.3:c.974T>A XP_005247446.1:p.Ile325Asn
XM_011512738.1:c.1070T>A XP_011511040.1:p.Ile357Asn
XM_011512739.1:c.533T>A XP_011511041.1:p.Ile178Asn
XM_005247389.4:c.974T>A XP_005247446.1:p.Ile325Asn
XM_011512738.2:c.1070T>A XP_011511040.1:p.Ile357Asn
XM_011512739.2:c.533T>A XP_011511041.1:p.Ile178Asn
NM_001199799.2:c.1070T>A MANE Select NP_001186728.1:p.Ile357Asn
NM_001199800.2:c.803T>A NP_001186729.1:p.Ile268Asn
NM_175924.4:c.938T>A NP_787120.1:p.Ile313Asn