Canonical Allele Identifier: CA354143452

Gene: ILDR1

Linked Data

• MyVariant Identifiers: chr3:g.121712410C>G (hg19) ; chr3:g.121993563C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993563C>G , CM000665.2:g.121993563C>G	GRCh38
NC_000003.11:g.121712410C>G , CM000665.1:g.121712410C>G	GRCh37
NC_000003.10:g.123195100C>G	NCBI36
NG_031870.1:g.33718G>C
NG_031870.2:g.71992G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1186G>C MANE Select	ENSP00000345667.5:p.Asp396His
ENST00000460554.2:n.1136G>C
ENST00000642615.1:c.*369G>C	ENSP00000495499.1:n.*369G>C
ENST00000273691.7:c.1054G>C	ENSP00000273691.3:p.Asp352His
ENST00000344209.9:c.1186G>C	ENSP00000345667.5:p.Asp396His
ENST00000393631.5:c.919G>C	ENSP00000377251.1:p.Asp307His
ENST00000460554.1:n.1288G>C
ENST00000462014.1:c.1090G>C	ENSP00000419414.1:p.Asp364His
NM_001199799.1:c.1186G>C	NP_001186728.1:p.Asp396His
NM_001199800.1:c.919G>C	NP_001186729.1:p.Asp307His
NM_175924.3:c.1054G>C	NP_787120.1:p.Asp352His
XM_005247389.3:c.1090G>C	XP_005247446.1:p.Asp364His
XM_011512738.1:c.1186G>C	XP_011511040.1:p.Asp396His
XM_011512739.1:c.649G>C	XP_011511041.1:p.Asp217His
XM_005247389.4:c.1090G>C	XP_005247446.1:p.Asp364His
XM_011512738.2:c.1186G>C	XP_011511040.1:p.Asp396His
XM_011512739.2:c.649G>C	XP_011511041.1:p.Asp217His
NM_001199799.2:c.1186G>C MANE Select	NP_001186728.1:p.Asp396His
NM_001199800.2:c.919G>C	NP_001186729.1:p.Asp307His
NM_175924.4:c.1054G>C	NP_787120.1:p.Asp352His