Canonical Allele Identifier: CA545640363
Gene: ILDR1 HGNC NCBI

Linked Data

dbSNP Id: rs1266174040

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122022183G>A , CM000665.2:g.122022183G>A GRCh38
NC_000003.11:g.121741030G>A , CM000665.1:g.121741030G>A GRCh37
NC_000003.10:g.123223720G>A NCBI36
NG_031870.1:g.5098C>T
NG_031870.2:g.43372C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.-106C>T MANE Select ENSP00000345667.5:n.-106C>T
ENST00000642615.1:c.-106C>T ENSP00000495499.1:n.-106C>T
ENST00000273691.7:c.-106C>T ENSP00000273691.3:n.-106C>T
ENST00000344209.9:c.-106C>T ENSP00000345667.5:n.-106C>T
ENST00000460554.1:n.16C>T
NM_001199799.1:c.-106C>T NP_001186728.1:n.-106C>T
NM_001199800.1:c.-106C>T NP_001186729.1:n.-106C>T
NM_175924.3:c.-106C>T NP_787120.1:n.-106C>T
XM_011512738.1:c.-106C>T XP_011511040.1:n.-106C>T
XM_011512739.1:c.-347-15022C>T XP_011511041.1:n.-347-15022C>T
XM_011512738.2:c.-106C>T XP_011511040.1:n.-106C>T
XM_011512739.2:c.-347-15022C>T XP_011511041.1:n.-347-15022C>T
NM_001199799.2:c.-106C>T MANE Select NP_001186728.1:n.-106C>T
NM_001199800.2:c.-106C>T NP_001186729.1:n.-106C>T
NM_175924.4:c.-106C>T NP_787120.1:n.-106C>T