Canonical Allele Identifier: CA412635806

Gene: IL1RAPL1

Linked Data

• MyVariant Identifiers: chrX:g.29935614T>G (hg19) ; chrX:g.29917497T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.29917497T>G , CM000685.2:g.29917497T>G	GRCh38
NC_000023.10:g.29935614T>G , CM000685.1:g.29935614T>G	GRCh37
NC_000023.9:g.29845535T>G	NCBI36
NG_008292.1:g.1334934T>G
NG_008292.2:g.1334934T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378993.6:c.812T>G MANE Select	ENSP00000368278.1:p.Phe271Cys
ENST00000302196.5:c.35T>G	ENSP00000305200.5:p.Phe12Cys
ENST00000378993.5:c.812T>G	ENSP00000368278.1:p.Phe271Cys
NM_014271.3:c.812T>G	NP_055086.1:p.Phe271Cys
XM_005274441.1:c.812T>G	XP_005274498.1:p.Phe271Cys
XM_011545445.1:c.812T>G	XP_011543747.1:p.Phe271Cys
XM_017029240.1:c.812T>G	XP_016884729.1:p.Phe271Cys
XM_017029241.1:c.434T>G	XP_016884730.1:p.Phe145Cys
NM_014271.4:c.812T>G MANE Select	NP_055086.1:p.Phe271Cys