Canonical Allele Identifier: CA354143905

Gene: ILDR1

Linked Data

• MyVariant Identifiers: chr3:g.121712496C>A (hg19) ; chr3:g.121993649C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993649C>A , CM000665.2:g.121993649C>A	GRCh38
NC_000003.11:g.121712496C>A , CM000665.1:g.121712496C>A	GRCh37
NC_000003.10:g.123195186C>A	NCBI36
NG_031870.1:g.33632G>T
NG_031870.2:g.71906G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1100G>T MANE Select	ENSP00000345667.5:p.Gly367Val
ENST00000460554.2:n.1050G>T
ENST00000642615.1:c.*283G>T	ENSP00000495499.1:n.*283G>T
ENST00000273691.7:c.968G>T	ENSP00000273691.3:p.Gly323Val
ENST00000344209.9:c.1100G>T	ENSP00000345667.5:p.Gly367Val
ENST00000393631.5:c.833G>T	ENSP00000377251.1:p.Gly278Val
ENST00000460554.1:n.1202G>T
ENST00000462014.1:c.1004G>T	ENSP00000419414.1:p.Gly335Val
NM_001199799.1:c.1100G>T	NP_001186728.1:p.Gly367Val
NM_001199800.1:c.833G>T	NP_001186729.1:p.Gly278Val
NM_175924.3:c.968G>T	NP_787120.1:p.Gly323Val
XM_005247389.3:c.1004G>T	XP_005247446.1:p.Gly335Val
XM_011512738.1:c.1100G>T	XP_011511040.1:p.Gly367Val
XM_011512739.1:c.563G>T	XP_011511041.1:p.Gly188Val
XM_005247389.4:c.1004G>T	XP_005247446.1:p.Gly335Val
XM_011512738.2:c.1100G>T	XP_011511040.1:p.Gly367Val
XM_011512739.2:c.563G>T	XP_011511041.1:p.Gly188Val
NM_001199799.2:c.1100G>T MANE Select	NP_001186728.1:p.Gly367Val
NM_001199800.2:c.833G>T	NP_001186729.1:p.Gly278Val
NM_175924.4:c.968G>T	NP_787120.1:p.Gly323Val