Canonical Allele Identifier: CA354144077

Gene: ILDR1

Linked Data

• MyVariant Identifiers: chr3:g.121712575A>T (hg19) ; chr3:g.121993728A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993728A>T , CM000665.2:g.121993728A>T	GRCh38
NC_000003.11:g.121712575A>T , CM000665.1:g.121712575A>T	GRCh37
NC_000003.10:g.123195265A>T	NCBI36
NG_031870.1:g.33553T>A
NG_031870.2:g.71827T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1021T>A MANE Select	ENSP00000345667.5:p.Ser341Thr
ENST00000460554.2:n.971T>A
ENST00000642615.1:c.*204T>A	ENSP00000495499.1:n.*204T>A
ENST00000273691.7:c.889T>A	ENSP00000273691.3:p.Ser297Thr
ENST00000344209.9:c.1021T>A	ENSP00000345667.5:p.Ser341Thr
ENST00000393631.5:c.754T>A	ENSP00000377251.1:p.Ser252Thr
ENST00000460554.1:n.1123T>A
ENST00000462014.1:c.925T>A	ENSP00000419414.1:p.Ser309Thr
NM_001199799.1:c.1021T>A	NP_001186728.1:p.Ser341Thr
NM_001199800.1:c.754T>A	NP_001186729.1:p.Ser252Thr
NM_175924.3:c.889T>A	NP_787120.1:p.Ser297Thr
XM_005247389.3:c.925T>A	XP_005247446.1:p.Ser309Thr
XM_011512738.1:c.1021T>A	XP_011511040.1:p.Ser341Thr
XM_011512739.1:c.484T>A	XP_011511041.1:p.Ser162Thr
XM_005247389.4:c.925T>A	XP_005247446.1:p.Ser309Thr
XM_011512738.2:c.1021T>A	XP_011511040.1:p.Ser341Thr
XM_011512739.2:c.484T>A	XP_011511041.1:p.Ser162Thr
NM_001199799.2:c.1021T>A MANE Select	NP_001186728.1:p.Ser341Thr
NM_001199800.2:c.754T>A	NP_001186729.1:p.Ser252Thr
NM_175924.4:c.889T>A	NP_787120.1:p.Ser297Thr