Canonical Allele Identifier: CA328261143

Gene: IL1RAPL1

Linked Data

• dbSNP Id: rs770642823
• gnomAD v2: X-29640756-C-T
• gnomAD v3: X-29622639-C-T
• gnomAD v4: X-29622639-C-T
• MyVariant Identifiers: chrX:g.29640756C>T (hg19) ; chrX:g.29622639C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.29622639C>T , CM000685.2:g.29622639C>T	GRCh38
NC_000023.10:g.29640756C>T , CM000685.1:g.29640756C>T	GRCh37
NC_000023.9:g.29550677C>T	NCBI36
NG_008292.1:g.1040076C>T
NG_008292.2:g.1040076C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378993.6:c.704-45791C>T MANE Select	ENSP00000368278.1:n.704-45791C>T
ENST00000378993.5:c.704-45791C>T	ENSP00000368278.1:n.704-45791C>T
NM_014271.3:c.704-45791C>T	NP_055086.1:n.704-45791C>T
XM_005274441.1:c.704-45791C>T	XP_005274498.1:n.704-45791C>T
XM_011545445.1:c.704-45791C>T	XP_011543747.1:n.704-45791C>T
XM_017029240.1:c.704-45791C>T	XP_016884729.1:n.704-45791C>T
XM_017029241.1:c.326-45791C>T	XP_016884730.1:n.326-45791C>T
NM_014271.4:c.704-45791C>T MANE Select	NP_055086.1:n.704-45791C>T