Canonical Allele Identifier: CA354142884

Gene: ILDR1

Linked Data

• MyVariant Identifiers: chr3:g.121712249C>G (hg19) ; chr3:g.121993402C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993402C>G , CM000665.2:g.121993402C>G	GRCh38
NC_000003.11:g.121712249C>G , CM000665.1:g.121712249C>G	GRCh37
NC_000003.10:g.123194939C>G	NCBI36
NG_031870.1:g.33879G>C
NG_031870.2:g.72153G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1347G>C MANE Select	ENSP00000345667.5:p.Arg449Ser
ENST00000460554.2:n.1297G>C
ENST00000642615.1:c.*530G>C	ENSP00000495499.1:n.*530G>C
ENST00000273691.7:c.1215G>C	ENSP00000273691.3:p.Arg405Ser
ENST00000344209.9:c.1347G>C	ENSP00000345667.5:p.Arg449Ser
ENST00000393631.5:c.1080G>C	ENSP00000377251.1:p.Arg360Ser
ENST00000460554.1:n.1449G>C
ENST00000462014.1:c.1251G>C	ENSP00000419414.1:p.Arg417Ser
NM_001199799.1:c.1347G>C	NP_001186728.1:p.Arg449Ser
NM_001199800.1:c.1080G>C	NP_001186729.1:p.Arg360Ser
NM_175924.3:c.1215G>C	NP_787120.1:p.Arg405Ser
XM_005247389.3:c.1251G>C	XP_005247446.1:p.Arg417Ser
XM_011512738.1:c.1347G>C	XP_011511040.1:p.Arg449Ser
XM_011512739.1:c.810G>C	XP_011511041.1:p.Arg270Ser
XM_005247389.4:c.1251G>C	XP_005247446.1:p.Arg417Ser
XM_011512738.2:c.1347G>C	XP_011511040.1:p.Arg449Ser
XM_011512739.2:c.810G>C	XP_011511041.1:p.Arg270Ser
NM_001199799.2:c.1347G>C MANE Select	NP_001186728.1:p.Arg449Ser
NM_001199800.2:c.1080G>C	NP_001186729.1:p.Arg360Ser
NM_175924.4:c.1215G>C	NP_787120.1:p.Arg405Ser