Canonical Allele Identifier: CA1397750706
Gene: ILDR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993214T= , CM000665.2:g.121993214T= GRCh38
NC_000003.11:g.121712061T= , CM000665.1:g.121712061T= GRCh37
NC_000003.10:g.123194751T= NCBI36
NG_031870.1:g.34067A=
NG_031870.2:g.72341A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1535A= MANE Select ENSP00000345667.5:p.Tyr512=
ENST00000460554.2:n.1485A=
ENST00000642615.1:c.*718A= ENSP00000495499.1:n.*718A=
ENST00000273691.7:c.1403A= ENSP00000273691.3:p.Tyr468=
ENST00000344209.9:c.1535A= ENSP00000345667.5:p.Tyr512=
ENST00000393631.5:c.1268A= ENSP00000377251.1:p.Tyr423=
ENST00000460554.1:n.1637A=
ENST00000462014.1:c.1439A= ENSP00000419414.1:p.Tyr480=
NM_001199799.1:c.1535A= NP_001186728.1:p.Tyr512=
NM_001199800.1:c.1268A= NP_001186729.1:p.Tyr423=
NM_175924.3:c.1403A= NP_787120.1:p.Tyr468=
XM_005247389.3:c.1439A= XP_005247446.1:p.Tyr480=
XM_011512738.1:c.1535A= XP_011511040.1:p.Tyr512=
XM_011512739.1:c.998A= XP_011511041.1:p.Tyr333=
XM_005247389.4:c.1439A= XP_005247446.1:p.Tyr480=
XM_011512738.2:c.1535A= XP_011511040.1:p.Tyr512=
XM_011512739.2:c.998A= XP_011511041.1:p.Tyr333=
NM_001199799.2:c.1535A= MANE Select NP_001186728.1:p.Tyr512=
NM_001199800.2:c.1268A= NP_001186729.1:p.Tyr423=
NM_175924.4:c.1403A= NP_787120.1:p.Tyr468=