Canonical Allele Identifier: CA515840428
Gene: IL1RAPL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.29417385A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.29399268A>C , CM000685.2:g.29399268A>C GRCh38
NC_000023.10:g.29417385A>C , CM000685.1:g.29417385A>C GRCh37
NC_000023.9:g.29327306A>C NCBI36
NG_008292.1:g.816705A>C
NG_008292.2:g.816705A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378993.6:c.663A>C MANE Select ENSP00000368278.1:p.Gly221=
ENST00000378993.5:c.663A>C ENSP00000368278.1:p.Gly221=
NM_014271.3:c.663A>C NP_055086.1:p.Gly221=
XM_005274441.1:c.663A>C XP_005274498.1:p.Gly221=
XM_011545445.1:c.663A>C XP_011543747.1:p.Gly221=
XM_017029240.1:c.663A>C XP_016884729.1:p.Gly221=
XM_017029241.1:c.285A>C XP_016884730.1:p.Gly95=
NM_014271.4:c.663A>C MANE Select NP_055086.1:p.Gly221=