Canonical Allele Identifier: CA1397763169

Gene: ILDR1

Linked Data

• dbSNP Id: rs2071866697

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122022117G>C , CM000665.2:g.122022117G>C	GRCh38
NC_000003.11:g.121740964G>C , CM000665.1:g.121740964G>C	GRCh37
NC_000003.10:g.123223654G>C	NCBI36
NG_031870.1:g.5164C>G
NG_031870.2:g.43438C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.-40C>G MANE Select	ENSP00000345667.5:n.-40C>G
ENST00000642615.1:c.-40C>G	ENSP00000495499.1:n.-40C>G
ENST00000273691.7:c.-40C>G	ENSP00000273691.3:n.-40C>G
ENST00000344209.9:c.-40C>G	ENSP00000345667.5:n.-40C>G
ENST00000393631.5:c.-40C>G	ENSP00000377251.1:n.-40C>G
ENST00000460554.1:n.82C>G
NM_001199799.1:c.-40C>G	NP_001186728.1:n.-40C>G
NM_001199800.1:c.-40C>G	NP_001186729.1:n.-40C>G
NM_175924.3:c.-40C>G	NP_787120.1:n.-40C>G
XM_011512738.1:c.-40C>G	XP_011511040.1:n.-40C>G
XM_011512739.1:c.-347-14956C>G	XP_011511041.1:n.-347-14956C>G
XM_011512738.2:c.-40C>G	XP_011511040.1:n.-40C>G
XM_011512739.2:c.-347-14956C>G	XP_011511041.1:n.-347-14956C>G
NM_001199799.2:c.-40C>G MANE Select	NP_001186728.1:n.-40C>G
NM_001199800.2:c.-40C>G	NP_001186729.1:n.-40C>G
NM_175924.4:c.-40C>G	NP_787120.1:n.-40C>G