Canonical Allele Identifier: CA354143074

Gene: ILDR1

Linked Data

• MyVariant Identifiers: chr3:g.121712301C>G (hg19) ; chr3:g.121993454C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993454C>G , CM000665.2:g.121993454C>G	GRCh38
NC_000003.11:g.121712301C>G , CM000665.1:g.121712301C>G	GRCh37
NC_000003.10:g.123194991C>G	NCBI36
NG_031870.1:g.33827G>C
NG_031870.2:g.72101G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1295G>C MANE Select	ENSP00000345667.5:p.Trp432Ser
ENST00000460554.2:n.1245G>C
ENST00000642615.1:c.*478G>C	ENSP00000495499.1:n.*478G>C
ENST00000273691.7:c.1163G>C	ENSP00000273691.3:p.Trp388Ser
ENST00000344209.9:c.1295G>C	ENSP00000345667.5:p.Trp432Ser
ENST00000393631.5:c.1028G>C	ENSP00000377251.1:p.Trp343Ser
ENST00000460554.1:n.1397G>C
ENST00000462014.1:c.1199G>C	ENSP00000419414.1:p.Trp400Ser
NM_001199799.1:c.1295G>C	NP_001186728.1:p.Trp432Ser
NM_001199800.1:c.1028G>C	NP_001186729.1:p.Trp343Ser
NM_175924.3:c.1163G>C	NP_787120.1:p.Trp388Ser
XM_005247389.3:c.1199G>C	XP_005247446.1:p.Trp400Ser
XM_011512738.1:c.1295G>C	XP_011511040.1:p.Trp432Ser
XM_011512739.1:c.758G>C	XP_011511041.1:p.Trp253Ser
XM_005247389.4:c.1199G>C	XP_005247446.1:p.Trp400Ser
XM_011512738.2:c.1295G>C	XP_011511040.1:p.Trp432Ser
XM_011512739.2:c.758G>C	XP_011511041.1:p.Trp253Ser
NM_001199799.2:c.1295G>C MANE Select	NP_001186728.1:p.Trp432Ser
NM_001199800.2:c.1028G>C	NP_001186729.1:p.Trp343Ser
NM_175924.4:c.1163G>C	NP_787120.1:p.Trp388Ser