Canonical Allele Identifier: CA435423767
Gene: ILDR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.121712335G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993488G>A , CM000665.2:g.121993488G>A GRCh38
NC_000003.11:g.121712335G>A , CM000665.1:g.121712335G>A GRCh37
NC_000003.10:g.123195025G>A NCBI36
NG_031870.1:g.33793C>T
NG_031870.2:g.72067C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000344209.10:c.1261C>T MANE Select ENSP00000345667.5:p.Leu421=
ENST00000460554.2:n.1211C>T
ENST00000642615.1:c.*444C>T ENSP00000495499.1:n.*444C>T
ENST00000273691.7:c.1129C>T ENSP00000273691.3:p.Leu377=
ENST00000344209.9:c.1261C>T ENSP00000345667.5:p.Leu421=
ENST00000393631.5:c.994C>T ENSP00000377251.1:p.Leu332=
ENST00000460554.1:n.1363C>T
ENST00000462014.1:c.1165C>T ENSP00000419414.1:p.Leu389=
NM_001199799.1:c.1261C>T NP_001186728.1:p.Leu421=
NM_001199800.1:c.994C>T NP_001186729.1:p.Leu332=
NM_175924.3:c.1129C>T NP_787120.1:p.Leu377=
XM_005247389.3:c.1165C>T XP_005247446.1:p.Leu389=
XM_011512738.1:c.1261C>T XP_011511040.1:p.Leu421=
XM_011512739.1:c.724C>T XP_011511041.1:p.Leu242=
XM_005247389.4:c.1165C>T XP_005247446.1:p.Leu389=
XM_011512738.2:c.1261C>T XP_011511040.1:p.Leu421=
XM_011512739.2:c.724C>T XP_011511041.1:p.Leu242=
NM_001199799.2:c.1261C>T MANE Select NP_001186728.1:p.Leu421=
NM_001199800.2:c.994C>T NP_001186729.1:p.Leu332=
NM_175924.4:c.1129C>T NP_787120.1:p.Leu377=