Canonical Allele Identifier: CA412635882

Gene: IL1RAPL1

Linked Data

• MyVariant Identifiers: chrX:g.29935647A>C (hg19) ; chrX:g.29917530A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.29917530A>C , CM000685.2:g.29917530A>C	GRCh38
NC_000023.10:g.29935647A>C , CM000685.1:g.29935647A>C	GRCh37
NC_000023.9:g.29845568A>C	NCBI36
NG_008292.1:g.1334967A>C
NG_008292.2:g.1334967A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378993.6:c.845A>C MANE Select	ENSP00000368278.1:p.Tyr282Ser
ENST00000302196.5:c.68A>C	ENSP00000305200.5:p.Tyr23Ser
ENST00000378993.5:c.845A>C	ENSP00000368278.1:p.Tyr282Ser
NM_014271.3:c.845A>C	NP_055086.1:p.Tyr282Ser
XM_005274441.1:c.845A>C	XP_005274498.1:p.Tyr282Ser
XM_011545445.1:c.845A>C	XP_011543747.1:p.Tyr282Ser
XM_017029240.1:c.845A>C	XP_016884729.1:p.Tyr282Ser
XM_017029241.1:c.467A>C	XP_016884730.1:p.Tyr156Ser
NM_014271.4:c.845A>C MANE Select	NP_055086.1:p.Tyr282Ser