Canonical Allele Identifier: CA874507177

Gene: IL1RAPL1

Linked Data

• dbSNP Id: rs1285038888
• gnomAD v3: X-29917698-A-G
• gnomAD v4: X-29917698-A-G
• MyVariant Identifiers: chrX:g.29935815A>G (hg19) ; chrX:g.29917698A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.29917698A>G , CM000685.2:g.29917698A>G	GRCh38
NC_000023.10:g.29935815A>G , CM000685.1:g.29935815A>G	GRCh37
NC_000023.9:g.29845736A>G	NCBI36
NG_008292.1:g.1335135A>G
NG_008292.2:g.1335135A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378993.6:c.911+102A>G MANE Select	ENSP00000368278.1:n.911+102A>G
ENST00000302196.5:c.134+102A>G	ENSP00000305200.5:n.134+102A>G
ENST00000378993.5:c.911+102A>G	ENSP00000368278.1:n.911+102A>G
NM_014271.3:c.911+102A>G	NP_055086.1:n.911+102A>G
XM_005274441.1:c.911+102A>G	XP_005274498.1:n.911+102A>G
XM_011545445.1:c.911+102A>G	XP_011543747.1:n.911+102A>G
XM_017029240.1:c.911+102A>G	XP_016884729.1:n.911+102A>G
XM_017029241.1:c.533+102A>G	XP_016884730.1:n.533+102A>G
NM_014271.4:c.911+102A>G MANE Select	NP_055086.1:n.911+102A>G