Canonical Allele Identifier: CA1397750683
Gene: ILDR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993175T= , CM000665.2:g.121993175T= GRCh38
NC_000003.11:g.121712022T= , CM000665.1:g.121712022T= GRCh37
NC_000003.10:g.123194712T= NCBI36
NG_031870.1:g.34106A=
NG_031870.2:g.72380A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1574A= MANE Select ENSP00000345667.5:p.Lys525=
ENST00000460554.2:n.1524A=
ENST00000642615.1:c.*757A= ENSP00000495499.1:n.*757A=
ENST00000273691.7:c.1442A= ENSP00000273691.3:p.Lys481=
ENST00000344209.9:c.1574A= ENSP00000345667.5:p.Lys525=
ENST00000393631.5:c.1307A= ENSP00000377251.1:p.Lys436=
ENST00000460554.1:n.1676A=
ENST00000462014.1:c.1478A= ENSP00000419414.1:p.Lys493=
NM_001199799.1:c.1574A= NP_001186728.1:p.Lys525=
NM_001199800.1:c.1307A= NP_001186729.1:p.Lys436=
NM_175924.3:c.1442A= NP_787120.1:p.Lys481=
XM_005247389.3:c.1478A= XP_005247446.1:p.Lys493=
XM_011512738.1:c.1558+16A= XP_011511040.1:n.1558+16A=
XM_011512739.1:c.1037A= XP_011511041.1:p.Lys346=
XM_005247389.4:c.1478A= XP_005247446.1:p.Lys493=
XM_011512738.2:c.1558+16A= XP_011511040.1:n.1558+16A=
XM_011512739.2:c.1037A= XP_011511041.1:p.Lys346=
NM_001199799.2:c.1574A= MANE Select NP_001186728.1:p.Lys525=
NM_001199800.2:c.1307A= NP_001186729.1:p.Lys436=
NM_175924.4:c.1442A= NP_787120.1:p.Lys481=