Canonical Allele Identifier: CA412635935

Gene: IL1RAPL1

Linked Data

• MyVariant Identifiers: chrX:g.29935668T>C (hg19) ; chrX:g.29917551T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.29917551T>C , CM000685.2:g.29917551T>C	GRCh38
NC_000023.10:g.29935668T>C , CM000685.1:g.29935668T>C	GRCh37
NC_000023.9:g.29845589T>C	NCBI36
NG_008292.1:g.1334988T>C
NG_008292.2:g.1334988T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378993.6:c.866T>C MANE Select	ENSP00000368278.1:p.Phe289Ser
ENST00000302196.5:c.89T>C	ENSP00000305200.5:p.Phe30Ser
ENST00000378993.5:c.866T>C	ENSP00000368278.1:p.Phe289Ser
NM_014271.3:c.866T>C	NP_055086.1:p.Phe289Ser
XM_005274441.1:c.866T>C	XP_005274498.1:p.Phe289Ser
XM_011545445.1:c.866T>C	XP_011543747.1:p.Phe289Ser
XM_017029240.1:c.866T>C	XP_016884729.1:p.Phe289Ser
XM_017029241.1:c.488T>C	XP_016884730.1:p.Phe163Ser
NM_014271.4:c.866T>C MANE Select	NP_055086.1:p.Phe289Ser