Canonical Allele Identifier: CA354144010

Gene: ILDR1

Linked Data

• MyVariant Identifiers: chr3:g.121712544T>C (hg19) ; chr3:g.121993697T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993697T>C , CM000665.2:g.121993697T>C	GRCh38
NC_000003.11:g.121712544T>C , CM000665.1:g.121712544T>C	GRCh37
NC_000003.10:g.123195234T>C	NCBI36
NG_031870.1:g.33584A>G
NG_031870.2:g.71858A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1052A>G MANE Select	ENSP00000345667.5:p.Gln351Arg
ENST00000460554.2:n.1002A>G
ENST00000642615.1:c.*235A>G	ENSP00000495499.1:n.*235A>G
ENST00000273691.7:c.920A>G	ENSP00000273691.3:p.Gln307Arg
ENST00000344209.9:c.1052A>G	ENSP00000345667.5:p.Gln351Arg
ENST00000393631.5:c.785A>G	ENSP00000377251.1:p.Gln262Arg
ENST00000460554.1:n.1154A>G
ENST00000462014.1:c.956A>G	ENSP00000419414.1:p.Gln319Arg
NM_001199799.1:c.1052A>G	NP_001186728.1:p.Gln351Arg
NM_001199800.1:c.785A>G	NP_001186729.1:p.Gln262Arg
NM_175924.3:c.920A>G	NP_787120.1:p.Gln307Arg
XM_005247389.3:c.956A>G	XP_005247446.1:p.Gln319Arg
XM_011512738.1:c.1052A>G	XP_011511040.1:p.Gln351Arg
XM_011512739.1:c.515A>G	XP_011511041.1:p.Gln172Arg
XM_005247389.4:c.956A>G	XP_005247446.1:p.Gln319Arg
XM_011512738.2:c.1052A>G	XP_011511040.1:p.Gln351Arg
XM_011512739.2:c.515A>G	XP_011511041.1:p.Gln172Arg
NM_001199799.2:c.1052A>G MANE Select	NP_001186728.1:p.Gln351Arg
NM_001199800.2:c.785A>G	NP_001186729.1:p.Gln262Arg
NM_175924.4:c.920A>G	NP_787120.1:p.Gln307Arg