Canonical Allele Identifier: CA354143978

Gene: ILDR1

Linked Data

• MyVariant Identifiers: chr3:g.121712529G>C (hg19) ; chr3:g.121993682G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993682G>C , CM000665.2:g.121993682G>C	GRCh38
NC_000003.11:g.121712529G>C , CM000665.1:g.121712529G>C	GRCh37
NC_000003.10:g.123195219G>C	NCBI36
NG_031870.1:g.33599C>G
NG_031870.2:g.71873C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1067C>G MANE Select	ENSP00000345667.5:p.Pro356Arg
ENST00000460554.2:n.1017C>G
ENST00000642615.1:c.*250C>G	ENSP00000495499.1:n.*250C>G
ENST00000273691.7:c.935C>G	ENSP00000273691.3:p.Pro312Arg
ENST00000344209.9:c.1067C>G	ENSP00000345667.5:p.Pro356Arg
ENST00000393631.5:c.800C>G	ENSP00000377251.1:p.Pro267Arg
ENST00000460554.1:n.1169C>G
ENST00000462014.1:c.971C>G	ENSP00000419414.1:p.Pro324Arg
NM_001199799.1:c.1067C>G	NP_001186728.1:p.Pro356Arg
NM_001199800.1:c.800C>G	NP_001186729.1:p.Pro267Arg
NM_175924.3:c.935C>G	NP_787120.1:p.Pro312Arg
XM_005247389.3:c.971C>G	XP_005247446.1:p.Pro324Arg
XM_011512738.1:c.1067C>G	XP_011511040.1:p.Pro356Arg
XM_011512739.1:c.530C>G	XP_011511041.1:p.Pro177Arg
XM_005247389.4:c.971C>G	XP_005247446.1:p.Pro324Arg
XM_011512738.2:c.1067C>G	XP_011511040.1:p.Pro356Arg
XM_011512739.2:c.530C>G	XP_011511041.1:p.Pro177Arg
NM_001199799.2:c.1067C>G MANE Select	NP_001186728.1:p.Pro356Arg
NM_001199800.2:c.800C>G	NP_001186729.1:p.Pro267Arg
NM_175924.4:c.935C>G	NP_787120.1:p.Pro312Arg