Canonical Allele Identifier: CA2667221378

Gene: ILDR1

Linked Data

• dbSNP Id: rs2107683704
• gnomAD v4: 3-122022194-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122022194C>A , CM000665.2:g.122022194C>A	GRCh38
NC_000003.11:g.121741041C>A , CM000665.1:g.121741041C>A	GRCh37
NC_000003.10:g.123223731C>A	NCBI36
NG_031870.1:g.5087G>T
NG_031870.2:g.43361G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.-117G>T MANE Select	ENSP00000345667.5:n.-117G>T
ENST00000642615.1:c.-117G>T	ENSP00000495499.1:n.-117G>T
ENST00000344209.9:c.-117G>T	ENSP00000345667.5:n.-117G>T
ENST00000460554.1:n.5G>T
NM_001199799.1:c.-117G>T	NP_001186728.1:n.-117G>T
NM_001199800.1:c.-117G>T	NP_001186729.1:n.-117G>T
NM_175924.3:c.-117G>T	NP_787120.1:n.-117G>T
XM_011512738.1:c.-117G>T	XP_011511040.1:n.-117G>T
XM_011512739.1:c.-347-15033G>T	XP_011511041.1:n.-347-15033G>T
XM_011512738.2:c.-117G>T	XP_011511040.1:n.-117G>T
XM_011512739.2:c.-347-15033G>T	XP_011511041.1:n.-347-15033G>T
NM_001199799.2:c.-117G>T MANE Select	NP_001186728.1:n.-117G>T
NM_001199800.2:c.-117G>T	NP_001186729.1:n.-117G>T
NM_175924.4:c.-117G>T	NP_787120.1:n.-117G>T