Canonical Allele Identifier: CA10375444
Gene: IL1RAPL1 HGNC NCBI

Linked Data

dbSNP Id: rs749083307
gnomAD v2: X-29417354-T-C
gnomAD v3: X-29399237-T-C
gnomAD v4: X-29399237-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.29399237T>C , CM000685.2:g.29399237T>C GRCh38
NC_000023.10:g.29417354T>C , CM000685.1:g.29417354T>C GRCh37
NC_000023.9:g.29327275T>C NCBI36
NG_008292.1:g.816674T>C
NG_008292.2:g.816674T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378993.6:c.632T>C MANE Select ENSP00000368278.1:p.Ile211Thr
ENST00000378993.5:c.632T>C ENSP00000368278.1:p.Ile211Thr
NM_014271.3:c.632T>C NP_055086.1:p.Ile211Thr
XM_005274441.1:c.632T>C XP_005274498.1:p.Ile211Thr
XM_011545445.1:c.632T>C XP_011543747.1:p.Ile211Thr
XM_017029240.1:c.632T>C XP_016884729.1:p.Ile211Thr
XM_017029241.1:c.254T>C XP_016884730.1:p.Ile85Thr
NM_014271.4:c.632T>C MANE Select NP_055086.1:p.Ile211Thr