Canonical Allele Identifier: CA10375452
Gene: IL1RAPL1 HGNC NCBI

Linked Data

dbSNP Id: rs765669133
ExAC: X:29417436 T / A
gnomAD v2: X-29417436-T-A
gnomAD v3: X-29399319-T-A
gnomAD v4: X-29399319-T-A
MyVariant Identifiers: chrX:g.29417436T>A (hg19) chrX:g.29399319T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.29399319T>A , CM000685.2:g.29399319T>A GRCh38
NC_000023.10:g.29417436T>A , CM000685.1:g.29417436T>A GRCh37
NC_000023.9:g.29327357T>A NCBI36
NG_008292.1:g.816756T>A
NG_008292.2:g.816756T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378993.6:c.703+11T>A MANE Select ENSP00000368278.1:n.703+11T>A
ENST00000378993.5:c.703+11T>A ENSP00000368278.1:n.703+11T>A
NM_014271.3:c.703+11T>A NP_055086.1:n.703+11T>A
XM_005274441.1:c.703+11T>A XP_005274498.1:n.703+11T>A
XM_011545445.1:c.703+11T>A XP_011543747.1:n.703+11T>A
XM_017029240.1:c.703+11T>A XP_016884729.1:n.703+11T>A
XM_017029241.1:c.325+11T>A XP_016884730.1:n.325+11T>A
NM_014271.4:c.703+11T>A MANE Select NP_055086.1:n.703+11T>A
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Search 100 bp 3'