Canonical Allele Identifier: CA898072770

Gene: ILDR1

Linked Data

• dbSNP Id: rs773296079
• gnomAD v4: 3-122022086-C-T
• MyVariant Identifiers: chr3:g.121740933C>T (hg19) ; chr3:g.122022086C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122022086C>T , CM000665.2:g.122022086C>T	GRCh38
NC_000003.11:g.121740933C>T , CM000665.1:g.121740933C>T	GRCh37
NC_000003.10:g.123223623C>T	NCBI36
NG_031870.1:g.5195G>A
NG_031870.2:g.43469G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.-9G>A MANE Select	ENSP00000345667.5:n.-9G>A
ENST00000642615.1:c.-9G>A	ENSP00000495499.1:n.-9G>A
ENST00000273691.7:c.-9G>A	ENSP00000273691.3:n.-9G>A
ENST00000344209.9:c.-9G>A	ENSP00000345667.5:n.-9G>A
ENST00000393631.5:c.-9G>A	ENSP00000377251.1:n.-9G>A
ENST00000460554.1:n.113G>A
NM_001199799.1:c.-9G>A	NP_001186728.1:n.-9G>A
NM_001199800.1:c.-9G>A	NP_001186729.1:n.-9G>A
NM_175924.3:c.-9G>A	NP_787120.1:n.-9G>A
XM_011512738.1:c.-9G>A	XP_011511040.1:n.-9G>A
XM_011512739.1:c.-347-14925G>A	XP_011511041.1:n.-347-14925G>A
XM_011512738.2:c.-9G>A	XP_011511040.1:n.-9G>A
XM_011512739.2:c.-347-14925G>A	XP_011511041.1:n.-347-14925G>A
NM_001199799.2:c.-9G>A MANE Select	NP_001186728.1:n.-9G>A
NM_001199800.2:c.-9G>A	NP_001186729.1:n.-9G>A
NM_175924.4:c.-9G>A	NP_787120.1:n.-9G>A