Canonical Allele Identifier: CA354143940

Gene: ILDR1

Linked Data

• MyVariant Identifiers: chr3:g.121712511C>T (hg19) ; chr3:g.121993664C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993664C>T , CM000665.2:g.121993664C>T	GRCh38
NC_000003.11:g.121712511C>T , CM000665.1:g.121712511C>T	GRCh37
NC_000003.10:g.123195201C>T	NCBI36
NG_031870.1:g.33617G>A
NG_031870.2:g.71891G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1085G>A MANE Select	ENSP00000345667.5:p.Trp362Ter
ENST00000460554.2:n.1035G>A
ENST00000642615.1:c.*268G>A	ENSP00000495499.1:n.*268G>A
ENST00000273691.7:c.953G>A	ENSP00000273691.3:p.Trp318Ter
ENST00000344209.9:c.1085G>A	ENSP00000345667.5:p.Trp362Ter
ENST00000393631.5:c.818G>A	ENSP00000377251.1:p.Trp273Ter
ENST00000460554.1:n.1187G>A
ENST00000462014.1:c.989G>A	ENSP00000419414.1:p.Trp330Ter
NM_001199799.1:c.1085G>A	NP_001186728.1:p.Trp362Ter
NM_001199800.1:c.818G>A	NP_001186729.1:p.Trp273Ter
NM_175924.3:c.953G>A	NP_787120.1:p.Trp318Ter
XM_005247389.3:c.989G>A	XP_005247446.1:p.Trp330Ter
XM_011512738.1:c.1085G>A	XP_011511040.1:p.Trp362Ter
XM_011512739.1:c.548G>A	XP_011511041.1:p.Trp183Ter
XM_005247389.4:c.989G>A	XP_005247446.1:p.Trp330Ter
XM_011512738.2:c.1085G>A	XP_011511040.1:p.Trp362Ter
XM_011512739.2:c.548G>A	XP_011511041.1:p.Trp183Ter
NM_001199799.2:c.1085G>A MANE Select	NP_001186728.1:p.Trp362Ter
NM_001199800.2:c.818G>A	NP_001186729.1:p.Trp273Ter
NM_175924.4:c.953G>A	NP_787120.1:p.Trp318Ter