Canonical Allele Identifier: CA354142531

Gene: ILDR1

Linked Data

• MyVariant Identifiers: chr3:g.121712164A>T (hg19) ; chr3:g.121993317A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993317A>T , CM000665.2:g.121993317A>T	GRCh38
NC_000003.11:g.121712164A>T , CM000665.1:g.121712164A>T	GRCh37
NC_000003.10:g.123194854A>T	NCBI36
NG_031870.1:g.33964T>A
NG_031870.2:g.72238T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1432T>A MANE Select	ENSP00000345667.5:p.Ser478Thr
ENST00000460554.2:n.1382T>A
ENST00000642615.1:c.*615T>A	ENSP00000495499.1:n.*615T>A
ENST00000273691.7:c.1300T>A	ENSP00000273691.3:p.Ser434Thr
ENST00000344209.9:c.1432T>A	ENSP00000345667.5:p.Ser478Thr
ENST00000393631.5:c.1165T>A	ENSP00000377251.1:p.Ser389Thr
ENST00000460554.1:n.1534T>A
ENST00000462014.1:c.1336T>A	ENSP00000419414.1:p.Ser446Thr
NM_001199799.1:c.1432T>A	NP_001186728.1:p.Ser478Thr
NM_001199800.1:c.1165T>A	NP_001186729.1:p.Ser389Thr
NM_175924.3:c.1300T>A	NP_787120.1:p.Ser434Thr
XM_005247389.3:c.1336T>A	XP_005247446.1:p.Ser446Thr
XM_011512738.1:c.1432T>A	XP_011511040.1:p.Ser478Thr
XM_011512739.1:c.895T>A	XP_011511041.1:p.Ser299Thr
XM_005247389.4:c.1336T>A	XP_005247446.1:p.Ser446Thr
XM_011512738.2:c.1432T>A	XP_011511040.1:p.Ser478Thr
XM_011512739.2:c.895T>A	XP_011511041.1:p.Ser299Thr
NM_001199799.2:c.1432T>A MANE Select	NP_001186728.1:p.Ser478Thr
NM_001199800.2:c.1165T>A	NP_001186729.1:p.Ser389Thr
NM_175924.4:c.1300T>A	NP_787120.1:p.Ser434Thr