Canonical Allele Identifier: CA435423690

Gene: ILDR1

Linked Data

• dbSNP Id: rs746959964
• gnomAD v2: 3-121712081-G-A
• gnomAD v3: 3-121993234-G-A
• gnomAD v4: 3-121993234-G-A
• MyVariant Identifiers: chr3:g.121712081G>A (hg19) ; chr3:g.121993234G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993234G>A , CM000665.2:g.121993234G>A	GRCh38
NC_000003.11:g.121712081G>A , CM000665.1:g.121712081G>A	GRCh37
NC_000003.10:g.123194771G>A	NCBI36
NG_031870.1:g.34047C>T
NG_031870.2:g.72321C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1515C>T MANE Select	ENSP00000345667.5:p.Pro505=
ENST00000460554.2:n.1465C>T
ENST00000642615.1:c.*698C>T	ENSP00000495499.1:n.*698C>T
ENST00000273691.7:c.1383C>T	ENSP00000273691.3:p.Pro461=
ENST00000344209.9:c.1515C>T	ENSP00000345667.5:p.Pro505=
ENST00000393631.5:c.1248C>T	ENSP00000377251.1:p.Pro416=
ENST00000460554.1:n.1617C>T
ENST00000462014.1:c.1419C>T	ENSP00000419414.1:p.Pro473=
NM_001199799.1:c.1515C>T	NP_001186728.1:p.Pro505=
NM_001199800.1:c.1248C>T	NP_001186729.1:p.Pro416=
NM_175924.3:c.1383C>T	NP_787120.1:p.Pro461=
XM_005247389.3:c.1419C>T	XP_005247446.1:p.Pro473=
XM_011512738.1:c.1515C>T	XP_011511040.1:p.Pro505=
XM_011512739.1:c.978C>T	XP_011511041.1:p.Pro326=
XM_005247389.4:c.1419C>T	XP_005247446.1:p.Pro473=
XM_011512738.2:c.1515C>T	XP_011511040.1:p.Pro505=
XM_011512739.2:c.978C>T	XP_011511041.1:p.Pro326=
NM_001199799.2:c.1515C>T MANE Select	NP_001186728.1:p.Pro505=
NM_001199800.2:c.1248C>T	NP_001186729.1:p.Pro416=
NM_175924.4:c.1383C>T	NP_787120.1:p.Pro461=