Canonical Allele Identifier: CA515840660
Gene: IL1RAPL1 HGNC NCBI

Linked Data

gnomAD v4: X-29917574-C-A
MyVariant Identifiers: chrX:g.29935691C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.29917574C>A , CM000685.2:g.29917574C>A GRCh38
NC_000023.10:g.29935691C>A , CM000685.1:g.29935691C>A GRCh37
NC_000023.9:g.29845612C>A NCBI36
NG_008292.1:g.1335011C>A
NG_008292.2:g.1335011C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378993.6:c.889C>A MANE Select ENSP00000368278.1:p.Arg297=
ENST00000302196.5:c.112C>A ENSP00000305200.5:p.Arg38=
ENST00000378993.5:c.889C>A ENSP00000368278.1:p.Arg297=
NM_014271.3:c.889C>A NP_055086.1:p.Arg297=
XM_005274441.1:c.889C>A XP_005274498.1:p.Arg297=
XM_011545445.1:c.889C>A XP_011543747.1:p.Arg297=
XM_017029240.1:c.889C>A XP_016884729.1:p.Arg297=
XM_017029241.1:c.511C>A XP_016884730.1:p.Arg171=
NM_014271.4:c.889C>A MANE Select NP_055086.1:p.Arg297=