Canonical Allele Identifier: CA1397763203
Gene: ILDR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122022181C= , CM000665.2:g.122022181C= GRCh38
NC_000003.11:g.121741028C= , CM000665.1:g.121741028C= GRCh37
NC_000003.10:g.123223718C= NCBI36
NG_031870.1:g.5100G=
NG_031870.2:g.43374G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.-104G= MANE Select ENSP00000345667.5:n.-104G=
ENST00000642615.1:c.-104G= ENSP00000495499.1:n.-104G=
ENST00000273691.7:c.-104G= ENSP00000273691.3:n.-104G=
ENST00000344209.9:c.-104G= ENSP00000345667.5:n.-104G=
ENST00000460554.1:n.18G=
NM_001199799.1:c.-104G= NP_001186728.1:n.-104G=
NM_001199800.1:c.-104G= NP_001186729.1:n.-104G=
NM_175924.3:c.-104G= NP_787120.1:n.-104G=
XM_011512738.1:c.-104G= XP_011511040.1:n.-104G=
XM_011512739.1:c.-347-15020G= XP_011511041.1:n.-347-15020G=
XM_011512738.2:c.-104G= XP_011511040.1:n.-104G=
XM_011512739.2:c.-347-15020G= XP_011511041.1:n.-347-15020G=
NM_001199799.2:c.-104G= MANE Select NP_001186728.1:n.-104G=
NM_001199800.2:c.-104G= NP_001186729.1:n.-104G=
NM_175924.4:c.-104G= NP_787120.1:n.-104G=