Canonical Allele Identifier: CA435423814
Gene: ILDR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.121712486G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993639G>A , CM000665.2:g.121993639G>A GRCh38
NC_000003.11:g.121712486G>A , CM000665.1:g.121712486G>A GRCh37
NC_000003.10:g.123195176G>A NCBI36
NG_031870.1:g.33642C>T
NG_031870.2:g.71916C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1110C>T MANE Select ENSP00000345667.5:p.His370=
ENST00000460554.2:n.1060C>T
ENST00000642615.1:c.*293C>T ENSP00000495499.1:n.*293C>T
ENST00000273691.7:c.978C>T ENSP00000273691.3:p.His326=
ENST00000344209.9:c.1110C>T ENSP00000345667.5:p.His370=
ENST00000393631.5:c.843C>T ENSP00000377251.1:p.His281=
ENST00000460554.1:n.1212C>T
ENST00000462014.1:c.1014C>T ENSP00000419414.1:p.His338=
NM_001199799.1:c.1110C>T NP_001186728.1:p.His370=
NM_001199800.1:c.843C>T NP_001186729.1:p.His281=
NM_175924.3:c.978C>T NP_787120.1:p.His326=
XM_005247389.3:c.1014C>T XP_005247446.1:p.His338=
XM_011512738.1:c.1110C>T XP_011511040.1:p.His370=
XM_011512739.1:c.573C>T XP_011511041.1:p.His191=
XM_005247389.4:c.1014C>T XP_005247446.1:p.His338=
XM_011512738.2:c.1110C>T XP_011511040.1:p.His370=
XM_011512739.2:c.573C>T XP_011511041.1:p.His191=
NM_001199799.2:c.1110C>T MANE Select NP_001186728.1:p.His370=
NM_001199800.2:c.843C>T NP_001186729.1:p.His281=
NM_175924.4:c.978C>T NP_787120.1:p.His326=