Canonical Allele Identifier: CA354143233

Gene: ILDR1

Linked Data

• MyVariant Identifiers: chr3:g.121712346T>A (hg19) ; chr3:g.121993499T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993499T>A , CM000665.2:g.121993499T>A	GRCh38
NC_000003.11:g.121712346T>A , CM000665.1:g.121712346T>A	GRCh37
NC_000003.10:g.123195036T>A	NCBI36
NG_031870.1:g.33782A>T
NG_031870.2:g.72056A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1250A>T MANE Select	ENSP00000345667.5:p.Asp417Val
ENST00000460554.2:n.1200A>T
ENST00000642615.1:c.*433A>T	ENSP00000495499.1:n.*433A>T
ENST00000273691.7:c.1118A>T	ENSP00000273691.3:p.Asp373Val
ENST00000344209.9:c.1250A>T	ENSP00000345667.5:p.Asp417Val
ENST00000393631.5:c.983A>T	ENSP00000377251.1:p.Asp328Val
ENST00000460554.1:n.1352A>T
ENST00000462014.1:c.1154A>T	ENSP00000419414.1:p.Asp385Val
NM_001199799.1:c.1250A>T	NP_001186728.1:p.Asp417Val
NM_001199800.1:c.983A>T	NP_001186729.1:p.Asp328Val
NM_175924.3:c.1118A>T	NP_787120.1:p.Asp373Val
XM_005247389.3:c.1154A>T	XP_005247446.1:p.Asp385Val
XM_011512738.1:c.1250A>T	XP_011511040.1:p.Asp417Val
XM_011512739.1:c.713A>T	XP_011511041.1:p.Asp238Val
XM_005247389.4:c.1154A>T	XP_005247446.1:p.Asp385Val
XM_011512738.2:c.1250A>T	XP_011511040.1:p.Asp417Val
XM_011512739.2:c.713A>T	XP_011511041.1:p.Asp238Val
NM_001199799.2:c.1250A>T MANE Select	NP_001186728.1:p.Asp417Val
NM_001199800.2:c.983A>T	NP_001186729.1:p.Asp328Val
NM_175924.4:c.1118A>T	NP_787120.1:p.Asp373Val