Canonical Allele Identifier: CA641153608

Gene: IL1RAPL1

Linked Data

• dbSNP Id: rs1410257545
• gnomAD v2: X-29935735-C-T
• gnomAD v3: X-29917618-C-T
• gnomAD v4: X-29917618-C-T
• MyVariant Identifiers: chrX:g.29935735C>T (hg19) ; chrX:g.29917618C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.29917618C>T , CM000685.2:g.29917618C>T	GRCh38
NC_000023.10:g.29935735C>T , CM000685.1:g.29935735C>T	GRCh37
NC_000023.9:g.29845656C>T	NCBI36
NG_008292.1:g.1335055C>T
NG_008292.2:g.1335055C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378993.6:c.911+22C>T MANE Select	ENSP00000368278.1:n.911+22C>T
ENST00000302196.5:c.134+22C>T	ENSP00000305200.5:n.134+22C>T
ENST00000378993.5:c.911+22C>T	ENSP00000368278.1:n.911+22C>T
NM_014271.3:c.911+22C>T	NP_055086.1:n.911+22C>T
XM_005274441.1:c.911+22C>T	XP_005274498.1:n.911+22C>T
XM_011545445.1:c.911+22C>T	XP_011543747.1:n.911+22C>T
XM_017029240.1:c.911+22C>T	XP_016884729.1:n.911+22C>T
XM_017029241.1:c.533+22C>T	XP_016884730.1:n.533+22C>T
NM_014271.4:c.911+22C>T MANE Select	NP_055086.1:n.911+22C>T