Canonical Allele Identifier: CA354143976
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993682G>A , CM000665.2:g.121993682G>A GRCh38
NC_000003.11:g.121712529G>A , CM000665.1:g.121712529G>A GRCh37
NC_000003.10:g.123195219G>A NCBI36
NG_031870.1:g.33599C>T
NG_031870.2:g.71873C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1067C>T MANE Select ENSP00000345667.5:p.Pro356Leu
ENST00000460554.2:n.1017C>T
ENST00000642615.1:c.*250C>T ENSP00000495499.1:n.*250C>T
ENST00000273691.7:c.935C>T ENSP00000273691.3:p.Pro312Leu
ENST00000344209.9:c.1067C>T ENSP00000345667.5:p.Pro356Leu
ENST00000393631.5:c.800C>T ENSP00000377251.1:p.Pro267Leu
ENST00000460554.1:n.1169C>T
ENST00000462014.1:c.971C>T ENSP00000419414.1:p.Pro324Leu
NM_001199799.1:c.1067C>T NP_001186728.1:p.Pro356Leu
NM_001199800.1:c.800C>T NP_001186729.1:p.Pro267Leu
NM_175924.3:c.935C>T NP_787120.1:p.Pro312Leu
XM_005247389.3:c.971C>T XP_005247446.1:p.Pro324Leu
XM_011512738.1:c.1067C>T XP_011511040.1:p.Pro356Leu
XM_011512739.1:c.530C>T XP_011511041.1:p.Pro177Leu
XM_005247389.4:c.971C>T XP_005247446.1:p.Pro324Leu
XM_011512738.2:c.1067C>T XP_011511040.1:p.Pro356Leu
XM_011512739.2:c.530C>T XP_011511041.1:p.Pro177Leu
NM_001199799.2:c.1067C>T MANE Select NP_001186728.1:p.Pro356Leu
NM_001199800.2:c.800C>T NP_001186729.1:p.Pro267Leu
NM_175924.4:c.935C>T NP_787120.1:p.Pro312Leu