Canonical Allele Identifier: CA354135947
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.122022031C>A , CM000665.2:g.122022031C>A GRCh38
NC_000003.11:g.121740878C>A , CM000665.1:g.121740878C>A GRCh37
NC_000003.10:g.123223568C>A NCBI36
NG_031870.1:g.5250G>T
NG_031870.2:g.43524G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.47G>T MANE Select ENSP00000345667.5:p.Trp16Leu
ENST00000642615.1:c.47G>T ENSP00000495499.1:p.Trp16Leu
ENST00000273691.7:c.47G>T ENSP00000273691.3:p.Trp16Leu
ENST00000344209.9:c.47G>T ENSP00000345667.5:p.Trp16Leu
ENST00000393631.5:c.47G>T ENSP00000377251.1:p.Trp16Leu
ENST00000460554.1:n.168G>T
NM_001199799.1:c.47G>T NP_001186728.1:p.Trp16Leu
NM_001199800.1:c.47G>T NP_001186729.1:p.Trp16Leu
NM_175924.3:c.47G>T NP_787120.1:p.Trp16Leu
XM_011512738.1:c.47G>T XP_011511040.1:p.Trp16Leu
XM_011512739.1:c.-347-14870G>T XP_011511041.1:n.-347-14870G>T
XM_011512738.2:c.47G>T XP_011511040.1:p.Trp16Leu
XM_011512739.2:c.-347-14870G>T XP_011511041.1:n.-347-14870G>T
NM_001199799.2:c.47G>T MANE Select NP_001186728.1:p.Trp16Leu
NM_001199800.2:c.47G>T NP_001186729.1:p.Trp16Leu
NM_175924.4:c.47G>T NP_787120.1:p.Trp16Leu