Canonical Allele Identifier: CA412632726

Gene: IL1RAPL1

Linked Data

• MyVariant Identifiers: chrX:g.29417390T>C (hg19) ; chrX:g.29399273T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.29399273T>C , CM000685.2:g.29399273T>C	GRCh38
NC_000023.10:g.29417390T>C , CM000685.1:g.29417390T>C	GRCh37
NC_000023.9:g.29327311T>C	NCBI36
NG_008292.1:g.816710T>C
NG_008292.2:g.816710T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378993.6:c.668T>C MANE Select	ENSP00000368278.1:p.Phe223Ser
ENST00000378993.5:c.668T>C	ENSP00000368278.1:p.Phe223Ser
NM_014271.3:c.668T>C	NP_055086.1:p.Phe223Ser
XM_005274441.1:c.668T>C	XP_005274498.1:p.Phe223Ser
XM_011545445.1:c.668T>C	XP_011543747.1:p.Phe223Ser
XM_017029240.1:c.668T>C	XP_016884729.1:p.Phe223Ser
XM_017029241.1:c.290T>C	XP_016884730.1:p.Phe97Ser
NM_014271.4:c.668T>C MANE Select	NP_055086.1:p.Phe223Ser