Canonical Allele Identifier: CA354144037
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993710C>A , CM000665.2:g.121993710C>A GRCh38
NC_000003.11:g.121712557C>A , CM000665.1:g.121712557C>A GRCh37
NC_000003.10:g.123195247C>A NCBI36
NG_031870.1:g.33571G>T
NG_031870.2:g.71845G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1039G>T MANE Select ENSP00000345667.5:p.Asp347Tyr
ENST00000460554.2:n.989G>T
ENST00000642615.1:c.*222G>T ENSP00000495499.1:n.*222G>T
ENST00000273691.7:c.907G>T ENSP00000273691.3:p.Asp303Tyr
ENST00000344209.9:c.1039G>T ENSP00000345667.5:p.Asp347Tyr
ENST00000393631.5:c.772G>T ENSP00000377251.1:p.Asp258Tyr
ENST00000460554.1:n.1141G>T
ENST00000462014.1:c.943G>T ENSP00000419414.1:p.Asp315Tyr
NM_001199799.1:c.1039G>T NP_001186728.1:p.Asp347Tyr
NM_001199800.1:c.772G>T NP_001186729.1:p.Asp258Tyr
NM_175924.3:c.907G>T NP_787120.1:p.Asp303Tyr
XM_005247389.3:c.943G>T XP_005247446.1:p.Asp315Tyr
XM_011512738.1:c.1039G>T XP_011511040.1:p.Asp347Tyr
XM_011512739.1:c.502G>T XP_011511041.1:p.Asp168Tyr
XM_005247389.4:c.943G>T XP_005247446.1:p.Asp315Tyr
XM_011512738.2:c.1039G>T XP_011511040.1:p.Asp347Tyr
XM_011512739.2:c.502G>T XP_011511041.1:p.Asp168Tyr
NM_001199799.2:c.1039G>T MANE Select NP_001186728.1:p.Asp347Tyr
NM_001199800.2:c.772G>T NP_001186729.1:p.Asp258Tyr
NM_175924.4:c.907G>T NP_787120.1:p.Asp303Tyr