Canonical Allele Identifier: CA435423792

Gene: ILDR1

Linked Data

• MyVariant Identifiers: chr3:g.121712363T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993516T>G , CM000665.2:g.121993516T>G	GRCh38
NC_000003.11:g.121712363T>G , CM000665.1:g.121712363T>G	GRCh37
NC_000003.10:g.123195053T>G	NCBI36
NG_031870.1:g.33765A>C
NG_031870.2:g.72039A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1233A>C MANE Select	ENSP00000345667.5:p.Ser411=
ENST00000460554.2:n.1183A>C
ENST00000642615.1:c.*416A>C	ENSP00000495499.1:n.*416A>C
ENST00000273691.7:c.1101A>C	ENSP00000273691.3:p.Ser367=
ENST00000344209.9:c.1233A>C	ENSP00000345667.5:p.Ser411=
ENST00000393631.5:c.966A>C	ENSP00000377251.1:p.Ser322=
ENST00000460554.1:n.1335A>C
ENST00000462014.1:c.1137A>C	ENSP00000419414.1:p.Ser379=
NM_001199799.1:c.1233A>C	NP_001186728.1:p.Ser411=
NM_001199800.1:c.966A>C	NP_001186729.1:p.Ser322=
NM_175924.3:c.1101A>C	NP_787120.1:p.Ser367=
XM_005247389.3:c.1137A>C	XP_005247446.1:p.Ser379=
XM_011512738.1:c.1233A>C	XP_011511040.1:p.Ser411=
XM_011512739.1:c.696A>C	XP_011511041.1:p.Ser232=
XM_005247389.4:c.1137A>C	XP_005247446.1:p.Ser379=
XM_011512738.2:c.1233A>C	XP_011511040.1:p.Ser411=
XM_011512739.2:c.696A>C	XP_011511041.1:p.Ser232=
NM_001199799.2:c.1233A>C MANE Select	NP_001186728.1:p.Ser411=
NM_001199800.2:c.966A>C	NP_001186729.1:p.Ser322=
NM_175924.4:c.1101A>C	NP_787120.1:p.Ser367=