Canonical Allele Identifier: CA354144031
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993707A>C , CM000665.2:g.121993707A>C GRCh38
NC_000003.11:g.121712554A>C , CM000665.1:g.121712554A>C GRCh37
NC_000003.10:g.123195244A>C NCBI36
NG_031870.1:g.33574T>G
NG_031870.2:g.71848T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1042T>G MANE Select ENSP00000345667.5:p.Ser348Ala
ENST00000460554.2:n.992T>G
ENST00000642615.1:c.*225T>G ENSP00000495499.1:n.*225T>G
ENST00000273691.7:c.910T>G ENSP00000273691.3:p.Ser304Ala
ENST00000344209.9:c.1042T>G ENSP00000345667.5:p.Ser348Ala
ENST00000393631.5:c.775T>G ENSP00000377251.1:p.Ser259Ala
ENST00000460554.1:n.1144T>G
ENST00000462014.1:c.946T>G ENSP00000419414.1:p.Ser316Ala
NM_001199799.1:c.1042T>G NP_001186728.1:p.Ser348Ala
NM_001199800.1:c.775T>G NP_001186729.1:p.Ser259Ala
NM_175924.3:c.910T>G NP_787120.1:p.Ser304Ala
XM_005247389.3:c.946T>G XP_005247446.1:p.Ser316Ala
XM_011512738.1:c.1042T>G XP_011511040.1:p.Ser348Ala
XM_011512739.1:c.505T>G XP_011511041.1:p.Ser169Ala
XM_005247389.4:c.946T>G XP_005247446.1:p.Ser316Ala
XM_011512738.2:c.1042T>G XP_011511040.1:p.Ser348Ala
XM_011512739.2:c.505T>G XP_011511041.1:p.Ser169Ala
NM_001199799.2:c.1042T>G MANE Select NP_001186728.1:p.Ser348Ala
NM_001199800.2:c.775T>G NP_001186729.1:p.Ser259Ala
NM_175924.4:c.910T>G NP_787120.1:p.Ser304Ala