Canonical Allele Identifier: CA354141877

Gene: ILDR1

Linked Data

• dbSNP Id: rs1202130617
• gnomAD v4: 3-121993194-G-C
• MyVariant Identifiers: chr3:g.121712041G>C (hg19) ; chr3:g.121993194G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993194G>C , CM000665.2:g.121993194G>C	GRCh38
NC_000003.11:g.121712041G>C , CM000665.1:g.121712041G>C	GRCh37
NC_000003.10:g.123194731G>C	NCBI36
NG_031870.1:g.34087C>G
NG_031870.2:g.72361C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1555C>G MANE Select	ENSP00000345667.5:p.Pro519Ala
ENST00000460554.2:n.1505C>G
ENST00000642615.1:c.*738C>G	ENSP00000495499.1:n.*738C>G
ENST00000273691.7:c.1423C>G	ENSP00000273691.3:p.Pro475Ala
ENST00000344209.9:c.1555C>G	ENSP00000345667.5:p.Pro519Ala
ENST00000393631.5:c.1288C>G	ENSP00000377251.1:p.Pro430Ala
ENST00000460554.1:n.1657C>G
ENST00000462014.1:c.1459C>G	ENSP00000419414.1:p.Pro487Ala
NM_001199799.1:c.1555C>G	NP_001186728.1:p.Pro519Ala
NM_001199800.1:c.1288C>G	NP_001186729.1:p.Pro430Ala
NM_175924.3:c.1423C>G	NP_787120.1:p.Pro475Ala
XM_005247389.3:c.1459C>G	XP_005247446.1:p.Pro487Ala
XM_011512738.1:c.1555C>G	XP_011511040.1:p.Pro519Ala
XM_011512739.1:c.1018C>G	XP_011511041.1:p.Pro340Ala
XM_005247389.4:c.1459C>G	XP_005247446.1:p.Pro487Ala
XM_011512738.2:c.1555C>G	XP_011511040.1:p.Pro519Ala
XM_011512739.2:c.1018C>G	XP_011511041.1:p.Pro340Ala
NM_001199799.2:c.1555C>G MANE Select	NP_001186728.1:p.Pro519Ala
NM_001199800.2:c.1288C>G	NP_001186729.1:p.Pro430Ala
NM_175924.4:c.1423C>G	NP_787120.1:p.Pro475Ala