Canonical Allele Identifier: CA515840657
Gene: IL1RAPL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.29935684T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.29917567T>C , CM000685.2:g.29917567T>C GRCh38
NC_000023.10:g.29935684T>C , CM000685.1:g.29935684T>C GRCh37
NC_000023.9:g.29845605T>C NCBI36
NG_008292.1:g.1335004T>C
NG_008292.2:g.1335004T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378993.6:c.882T>C MANE Select ENSP00000368278.1:p.Asp294=
ENST00000302196.5:c.105T>C ENSP00000305200.5:p.Asp35=
ENST00000378993.5:c.882T>C ENSP00000368278.1:p.Asp294=
NM_014271.3:c.882T>C NP_055086.1:p.Asp294=
XM_005274441.1:c.882T>C XP_005274498.1:p.Asp294=
XM_011545445.1:c.882T>C XP_011543747.1:p.Asp294=
XM_017029240.1:c.882T>C XP_016884729.1:p.Asp294=
XM_017029241.1:c.504T>C XP_016884730.1:p.Asp168=
NM_014271.4:c.882T>C MANE Select NP_055086.1:p.Asp294=