Canonical Allele Identifier: CA641145685
Gene: IL1RAPL1 HGNC NCBI

Linked Data

dbSNP Id: rs1254589126
gnomAD v2: X-29640714-C-A
gnomAD v3: X-29622597-C-A
gnomAD v4: X-29622597-C-A
MyVariant Identifiers: chrX:g.29640714C>A (hg19) chrX:g.29622597C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.29622597C>A , CM000685.2:g.29622597C>A GRCh38
NC_000023.10:g.29640714C>A , CM000685.1:g.29640714C>A GRCh37
NC_000023.9:g.29550635C>A NCBI36
NG_008292.1:g.1040034C>A
NG_008292.2:g.1040034C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378993.6:c.704-45833C>A MANE Select ENSP00000368278.1:n.704-45833C>A
ENST00000378993.5:c.704-45833C>A ENSP00000368278.1:n.704-45833C>A
NM_014271.3:c.704-45833C>A NP_055086.1:n.704-45833C>A
XM_005274441.1:c.704-45833C>A XP_005274498.1:n.704-45833C>A
XM_011545445.1:c.704-45833C>A XP_011543747.1:n.704-45833C>A
XM_017029240.1:c.704-45833C>A XP_016884729.1:n.704-45833C>A
XM_017029241.1:c.326-45833C>A XP_016884730.1:n.326-45833C>A
NM_014271.4:c.704-45833C>A MANE Select NP_055086.1:n.704-45833C>A
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