Canonical Allele Identifier: CA435423752

Gene: ILDR1

Linked Data

• MyVariant Identifiers: chr3:g.121712186A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993339A>C , CM000665.2:g.121993339A>C	GRCh38
NC_000003.11:g.121712186A>C , CM000665.1:g.121712186A>C	GRCh37
NC_000003.10:g.123194876A>C	NCBI36
NG_031870.1:g.33942T>G
NG_031870.2:g.72216T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1410T>G MANE Select	ENSP00000345667.5:p.Pro470=
ENST00000460554.2:n.1360T>G
ENST00000642615.1:c.*593T>G	ENSP00000495499.1:n.*593T>G
ENST00000273691.7:c.1278T>G	ENSP00000273691.3:p.Pro426=
ENST00000344209.9:c.1410T>G	ENSP00000345667.5:p.Pro470=
ENST00000393631.5:c.1143T>G	ENSP00000377251.1:p.Pro381=
ENST00000460554.1:n.1512T>G
ENST00000462014.1:c.1314T>G	ENSP00000419414.1:p.Pro438=
NM_001199799.1:c.1410T>G	NP_001186728.1:p.Pro470=
NM_001199800.1:c.1143T>G	NP_001186729.1:p.Pro381=
NM_175924.3:c.1278T>G	NP_787120.1:p.Pro426=
XM_005247389.3:c.1314T>G	XP_005247446.1:p.Pro438=
XM_011512738.1:c.1410T>G	XP_011511040.1:p.Pro470=
XM_011512739.1:c.873T>G	XP_011511041.1:p.Pro291=
XM_005247389.4:c.1314T>G	XP_005247446.1:p.Pro438=
XM_011512738.2:c.1410T>G	XP_011511040.1:p.Pro470=
XM_011512739.2:c.873T>G	XP_011511041.1:p.Pro291=
NM_001199799.2:c.1410T>G MANE Select	NP_001186728.1:p.Pro470=
NM_001199800.2:c.1143T>G	NP_001186729.1:p.Pro381=
NM_175924.4:c.1278T>G	NP_787120.1:p.Pro426=