Canonical Allele Identifier: CA1397750906
Gene: ILDR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993595G= , CM000665.2:g.121993595G= GRCh38
NC_000003.11:g.121712442G= , CM000665.1:g.121712442G= GRCh37
NC_000003.10:g.123195132G= NCBI36
NG_031870.1:g.33686C=
NG_031870.2:g.71960C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1154C= MANE Select ENSP00000345667.5:p.Pro385=
ENST00000460554.2:n.1104C=
ENST00000642615.1:c.*337C= ENSP00000495499.1:n.*337C=
ENST00000273691.7:c.1022C= ENSP00000273691.3:p.Pro341=
ENST00000344209.9:c.1154C= ENSP00000345667.5:p.Pro385=
ENST00000393631.5:c.887C= ENSP00000377251.1:p.Pro296=
ENST00000460554.1:n.1256C=
ENST00000462014.1:c.1058C= ENSP00000419414.1:p.Pro353=
NM_001199799.1:c.1154C= NP_001186728.1:p.Pro385=
NM_001199800.1:c.887C= NP_001186729.1:p.Pro296=
NM_175924.3:c.1022C= NP_787120.1:p.Pro341=
XM_005247389.3:c.1058C= XP_005247446.1:p.Pro353=
XM_011512738.1:c.1154C= XP_011511040.1:p.Pro385=
XM_011512739.1:c.617C= XP_011511041.1:p.Pro206=
XM_005247389.4:c.1058C= XP_005247446.1:p.Pro353=
XM_011512738.2:c.1154C= XP_011511040.1:p.Pro385=
XM_011512739.2:c.617C= XP_011511041.1:p.Pro206=
NM_001199799.2:c.1154C= MANE Select NP_001186728.1:p.Pro385=
NM_001199800.2:c.887C= NP_001186729.1:p.Pro296=
NM_175924.4:c.1022C= NP_787120.1:p.Pro341=