Canonical Allele Identifier: CA354144044
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993712C>T , CM000665.2:g.121993712C>T GRCh38
NC_000003.11:g.121712559C>T , CM000665.1:g.121712559C>T GRCh37
NC_000003.10:g.123195249C>T NCBI36
NG_031870.1:g.33569G>A
NG_031870.2:g.71843G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1037G>A MANE Select ENSP00000345667.5:p.Ser346Asn
ENST00000460554.2:n.987G>A
ENST00000642615.1:c.*220G>A ENSP00000495499.1:n.*220G>A
ENST00000273691.7:c.905G>A ENSP00000273691.3:p.Ser302Asn
ENST00000344209.9:c.1037G>A ENSP00000345667.5:p.Ser346Asn
ENST00000393631.5:c.770G>A ENSP00000377251.1:p.Ser257Asn
ENST00000460554.1:n.1139G>A
ENST00000462014.1:c.941G>A ENSP00000419414.1:p.Ser314Asn
NM_001199799.1:c.1037G>A NP_001186728.1:p.Ser346Asn
NM_001199800.1:c.770G>A NP_001186729.1:p.Ser257Asn
NM_175924.3:c.905G>A NP_787120.1:p.Ser302Asn
XM_005247389.3:c.941G>A XP_005247446.1:p.Ser314Asn
XM_011512738.1:c.1037G>A XP_011511040.1:p.Ser346Asn
XM_011512739.1:c.500G>A XP_011511041.1:p.Ser167Asn
XM_005247389.4:c.941G>A XP_005247446.1:p.Ser314Asn
XM_011512738.2:c.1037G>A XP_011511040.1:p.Ser346Asn
XM_011512739.2:c.500G>A XP_011511041.1:p.Ser167Asn
NM_001199799.2:c.1037G>A MANE Select NP_001186728.1:p.Ser346Asn
NM_001199800.2:c.770G>A NP_001186729.1:p.Ser257Asn
NM_175924.4:c.905G>A NP_787120.1:p.Ser302Asn