Canonical Allele Identifier: CA2577869687
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122022169C>A , CM000665.2:g.122022169C>A GRCh38
NC_000003.11:g.121741016C>A , CM000665.1:g.121741016C>A GRCh37
NC_000003.10:g.123223706C>A NCBI36
NG_031870.1:g.5112G>T
NG_031870.2:g.43386G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.-92G>T MANE Select ENSP00000345667.5:n.-92G>T
ENST00000642615.1:c.-92G>T ENSP00000495499.1:n.-92G>T
ENST00000273691.7:c.-92G>T ENSP00000273691.3:n.-92G>T
ENST00000344209.9:c.-92G>T ENSP00000345667.5:n.-92G>T
ENST00000460554.1:n.30G>T
NM_001199799.1:c.-92G>T NP_001186728.1:n.-92G>T
NM_001199800.1:c.-92G>T NP_001186729.1:n.-92G>T
NM_175924.3:c.-92G>T NP_787120.1:n.-92G>T
XM_011512738.1:c.-92G>T XP_011511040.1:n.-92G>T
XM_011512739.1:c.-347-15008G>T XP_011511041.1:n.-347-15008G>T
XM_011512738.2:c.-92G>T XP_011511040.1:n.-92G>T
XM_011512739.2:c.-347-15008G>T XP_011511041.1:n.-347-15008G>T
NM_001199799.2:c.-92G>T MANE Select NP_001186728.1:n.-92G>T
NM_001199800.2:c.-92G>T NP_001186729.1:n.-92G>T
NM_175924.4:c.-92G>T NP_787120.1:n.-92G>T