Canonical Allele Identifier: CA641153616

Gene: IL1RAPL1

Linked Data

• dbSNP Id: rs1329226447
• gnomAD v2: X-29935753-C-T
• gnomAD v3: X-29917636-C-T
• gnomAD v4: X-29917636-C-T
• MyVariant Identifiers: chrX:g.29935753C>T (hg19) ; chrX:g.29917636C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.29917636C>T , CM000685.2:g.29917636C>T	GRCh38
NC_000023.10:g.29935753C>T , CM000685.1:g.29935753C>T	GRCh37
NC_000023.9:g.29845674C>T	NCBI36
NG_008292.1:g.1335073C>T
NG_008292.2:g.1335073C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378993.6:c.911+40C>T MANE Select	ENSP00000368278.1:n.911+40C>T
ENST00000302196.5:c.134+40C>T	ENSP00000305200.5:n.134+40C>T
ENST00000378993.5:c.911+40C>T	ENSP00000368278.1:n.911+40C>T
NM_014271.3:c.911+40C>T	NP_055086.1:n.911+40C>T
XM_005274441.1:c.911+40C>T	XP_005274498.1:n.911+40C>T
XM_011545445.1:c.911+40C>T	XP_011543747.1:n.911+40C>T
XM_017029240.1:c.911+40C>T	XP_016884729.1:n.911+40C>T
XM_017029241.1:c.533+40C>T	XP_016884730.1:n.533+40C>T
NM_014271.4:c.911+40C>T MANE Select	NP_055086.1:n.911+40C>T