Canonical Allele Identifier: CA354143463
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993566A>C , CM000665.2:g.121993566A>C GRCh38
NC_000003.11:g.121712413A>C , CM000665.1:g.121712413A>C GRCh37
NC_000003.10:g.123195103A>C NCBI36
NG_031870.1:g.33715T>G
NG_031870.2:g.71989T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1183T>G MANE Select ENSP00000345667.5:p.Leu395Val
ENST00000460554.2:n.1133T>G
ENST00000642615.1:c.*366T>G ENSP00000495499.1:n.*366T>G
ENST00000273691.7:c.1051T>G ENSP00000273691.3:p.Leu351Val
ENST00000344209.9:c.1183T>G ENSP00000345667.5:p.Leu395Val
ENST00000393631.5:c.916T>G ENSP00000377251.1:p.Leu306Val
ENST00000460554.1:n.1285T>G
ENST00000462014.1:c.1087T>G ENSP00000419414.1:p.Leu363Val
NM_001199799.1:c.1183T>G NP_001186728.1:p.Leu395Val
NM_001199800.1:c.916T>G NP_001186729.1:p.Leu306Val
NM_175924.3:c.1051T>G NP_787120.1:p.Leu351Val
XM_005247389.3:c.1087T>G XP_005247446.1:p.Leu363Val
XM_011512738.1:c.1183T>G XP_011511040.1:p.Leu395Val
XM_011512739.1:c.646T>G XP_011511041.1:p.Leu216Val
XM_005247389.4:c.1087T>G XP_005247446.1:p.Leu363Val
XM_011512738.2:c.1183T>G XP_011511040.1:p.Leu395Val
XM_011512739.2:c.646T>G XP_011511041.1:p.Leu216Val
NM_001199799.2:c.1183T>G MANE Select NP_001186728.1:p.Leu395Val
NM_001199800.2:c.916T>G NP_001186729.1:p.Leu306Val
NM_175924.4:c.1051T>G NP_787120.1:p.Leu351Val