Canonical Allele Identifier: CA354143898

Gene: ILDR1

Linked Data

• MyVariant Identifiers: chr3:g.121712492T>A (hg19) ; chr3:g.121993645T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993645T>A , CM000665.2:g.121993645T>A	GRCh38
NC_000003.11:g.121712492T>A , CM000665.1:g.121712492T>A	GRCh37
NC_000003.10:g.123195182T>A	NCBI36
NG_031870.1:g.33636A>T
NG_031870.2:g.71910A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1104A>T MANE Select	ENSP00000345667.5:p.Arg368Ser
ENST00000460554.2:n.1054A>T
ENST00000642615.1:c.*287A>T	ENSP00000495499.1:n.*287A>T
ENST00000273691.7:c.972A>T	ENSP00000273691.3:p.Arg324Ser
ENST00000344209.9:c.1104A>T	ENSP00000345667.5:p.Arg368Ser
ENST00000393631.5:c.837A>T	ENSP00000377251.1:p.Arg279Ser
ENST00000460554.1:n.1206A>T
ENST00000462014.1:c.1008A>T	ENSP00000419414.1:p.Arg336Ser
NM_001199799.1:c.1104A>T	NP_001186728.1:p.Arg368Ser
NM_001199800.1:c.837A>T	NP_001186729.1:p.Arg279Ser
NM_175924.3:c.972A>T	NP_787120.1:p.Arg324Ser
XM_005247389.3:c.1008A>T	XP_005247446.1:p.Arg336Ser
XM_011512738.1:c.1104A>T	XP_011511040.1:p.Arg368Ser
XM_011512739.1:c.567A>T	XP_011511041.1:p.Arg189Ser
XM_005247389.4:c.1008A>T	XP_005247446.1:p.Arg336Ser
XM_011512738.2:c.1104A>T	XP_011511040.1:p.Arg368Ser
XM_011512739.2:c.567A>T	XP_011511041.1:p.Arg189Ser
NM_001199799.2:c.1104A>T MANE Select	NP_001186728.1:p.Arg368Ser
NM_001199800.2:c.837A>T	NP_001186729.1:p.Arg279Ser
NM_175924.4:c.972A>T	NP_787120.1:p.Arg324Ser