Canonical Allele Identifier: CA874507172

Gene: IL1RAPL1

Linked Data

• dbSNP Id: rs1217829548
• gnomAD v3: X-29917693-G-C
• gnomAD v4: X-29917693-G-C
• MyVariant Identifiers: chrX:g.29935810G>C (hg19) ; chrX:g.29917693G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.29917693G>C , CM000685.2:g.29917693G>C	GRCh38
NC_000023.10:g.29935810G>C , CM000685.1:g.29935810G>C	GRCh37
NC_000023.9:g.29845731G>C	NCBI36
NG_008292.1:g.1335130G>C
NG_008292.2:g.1335130G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378993.6:c.911+97G>C MANE Select	ENSP00000368278.1:n.911+97G>C
ENST00000302196.5:c.134+97G>C	ENSP00000305200.5:n.134+97G>C
ENST00000378993.5:c.911+97G>C	ENSP00000368278.1:n.911+97G>C
NM_014271.3:c.911+97G>C	NP_055086.1:n.911+97G>C
XM_005274441.1:c.911+97G>C	XP_005274498.1:n.911+97G>C
XM_011545445.1:c.911+97G>C	XP_011543747.1:n.911+97G>C
XM_017029240.1:c.911+97G>C	XP_016884729.1:n.911+97G>C
XM_017029241.1:c.533+97G>C	XP_016884730.1:n.533+97G>C
NM_014271.4:c.911+97G>C MANE Select	NP_055086.1:n.911+97G>C