Canonical Allele Identifier: CA515840623
Gene: IL1RAPL1 HGNC NCBI

Linked Data

gnomAD v4: X-29917495-C-T
MyVariant Identifiers: chrX:g.29935612C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.29917495C>T , CM000685.2:g.29917495C>T GRCh38
NC_000023.10:g.29935612C>T , CM000685.1:g.29935612C>T GRCh37
NC_000023.9:g.29845533C>T NCBI36
NG_008292.1:g.1334932C>T
NG_008292.2:g.1334932C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378993.6:c.810C>T MANE Select ENSP00000368278.1:p.Phe270=
ENST00000302196.5:c.33C>T ENSP00000305200.5:p.Phe11=
ENST00000378993.5:c.810C>T ENSP00000368278.1:p.Phe270=
NM_014271.3:c.810C>T NP_055086.1:p.Phe270=
XM_005274441.1:c.810C>T XP_005274498.1:p.Phe270=
XM_011545445.1:c.810C>T XP_011543747.1:p.Phe270=
XM_017029240.1:c.810C>T XP_016884729.1:p.Phe270=
XM_017029241.1:c.432C>T XP_016884730.1:p.Phe144=
NM_014271.4:c.810C>T MANE Select NP_055086.1:p.Phe270=