Canonical Allele Identifier: CA515840622
Gene: IL1RAPL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.29935609T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.29917492T>G , CM000685.2:g.29917492T>G GRCh38
NC_000023.10:g.29935609T>G , CM000685.1:g.29935609T>G GRCh37
NC_000023.9:g.29845530T>G NCBI36
NG_008292.1:g.1334929T>G
NG_008292.2:g.1334929T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378993.6:c.807T>G MANE Select ENSP00000368278.1:p.Ala269=
ENST00000302196.5:c.30T>G ENSP00000305200.5:p.Ala10=
ENST00000378993.5:c.807T>G ENSP00000368278.1:p.Ala269=
NM_014271.3:c.807T>G NP_055086.1:p.Ala269=
XM_005274441.1:c.807T>G XP_005274498.1:p.Ala269=
XM_011545445.1:c.807T>G XP_011543747.1:p.Ala269=
XM_017029240.1:c.807T>G XP_016884729.1:p.Ala269=
XM_017029241.1:c.429T>G XP_016884730.1:p.Ala143=
NM_014271.4:c.807T>G MANE Select NP_055086.1:p.Ala269=