Canonical Allele Identifier: CA2568741

Gene: ILDR1

Linked Data

• ClinVar Variation Id: 1898104
• ClinVar RCV Id: RCV002573772
• dbSNP Id: rs759613864
• ExAC: 3:121712386 G / T
• gnomAD v2: 3-121712386-G-T
• gnomAD v3: 3-121993539-G-T
• gnomAD v4: 3-121993539-G-T
• MyVariant Identifiers: chr3:g.121712386G>T (hg19) ; chr3:g.121993539G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993539G>T , CM000665.2:g.121993539G>T	GRCh38
NC_000003.11:g.121712386G>T , CM000665.1:g.121712386G>T	GRCh37
NC_000003.10:g.123195076G>T	NCBI36
NG_031870.1:g.33742C>A
NG_031870.2:g.72016C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1210C>A MANE Select	ENSP00000345667.5:p.Arg404Ser
ENST00000460554.2:n.1160C>A
ENST00000642615.1:c.*393C>A	ENSP00000495499.1:n.*393C>A
ENST00000273691.7:c.1078C>A	ENSP00000273691.3:p.Arg360Ser
ENST00000344209.9:c.1210C>A	ENSP00000345667.5:p.Arg404Ser
ENST00000393631.5:c.943C>A	ENSP00000377251.1:p.Arg315Ser
ENST00000460554.1:n.1312C>A
ENST00000462014.1:c.1114C>A	ENSP00000419414.1:p.Arg372Ser
NM_001199799.1:c.1210C>A	NP_001186728.1:p.Arg404Ser
NM_001199800.1:c.943C>A	NP_001186729.1:p.Arg315Ser
NM_175924.3:c.1078C>A	NP_787120.1:p.Arg360Ser
XM_005247389.3:c.1114C>A	XP_005247446.1:p.Arg372Ser
XM_011512738.1:c.1210C>A	XP_011511040.1:p.Arg404Ser
XM_011512739.1:c.673C>A	XP_011511041.1:p.Arg225Ser
XM_005247389.4:c.1114C>A	XP_005247446.1:p.Arg372Ser
XM_011512738.2:c.1210C>A	XP_011511040.1:p.Arg404Ser
XM_011512739.2:c.673C>A	XP_011511041.1:p.Arg225Ser
NM_001199799.2:c.1210C>A MANE Select	NP_001186728.1:p.Arg404Ser
NM_001199800.2:c.943C>A	NP_001186729.1:p.Arg315Ser
NM_175924.4:c.1078C>A	NP_787120.1:p.Arg360Ser