Canonical Allele Identifier: CA328286116
Gene: IL1RAPL1 HGNC NCBI

Linked Data

dbSNP Id: rs896568535
gnomAD v3: X-29917355-G-C
gnomAD v4: X-29917355-G-C
MyVariant Identifiers: chrX:g.29917355G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.29917355G>C , CM000685.2:g.29917355G>C GRCh38
NC_000023.10:g.29935472G>C , CM000685.1:g.29935472G>C GRCh37
NC_000023.9:g.29845393G>C NCBI36
NG_008292.1:g.1334792G>C
NG_008292.2:g.1334792G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378993.6:c.779-109G>C MANE Select ENSP00000368278.1:n.779-109G>C
ENST00000378993.5:c.779-109G>C ENSP00000368278.1:n.779-109G>C
NM_014271.3:c.779-109G>C NP_055086.1:n.779-109G>C
XM_005274441.1:c.779-109G>C XP_005274498.1:n.779-109G>C
XM_011545445.1:c.779-109G>C XP_011543747.1:n.779-109G>C
XM_017029240.1:c.779-109G>C XP_016884729.1:n.779-109G>C
XM_017029241.1:c.401-109G>C XP_016884730.1:n.401-109G>C
NM_014271.4:c.779-109G>C MANE Select NP_055086.1:n.779-109G>C