Canonical Allele Identifier: CA2576895810
Gene: IL11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55368504dup , CM000681.2:g.55368504dup GRCh38
NC_000019.9:g.55879872dup , CM000681.1:g.55879872dup GRCh37
NC_000019.8:g.60571684dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000264563.7:c.250dup MANE Select ENSP00000264563.1:p.Ala84GlyfsTer?
ENST00000264563.6:c.250dup ENSP00000264563.1:p.Ala84GlyfsTer?
ENST00000585513.1:c.250dup ENSP00000467355.1:p.Ala84GlyfsTer?
ENST00000587093.1:c.13dup ENSP00000468663.1:p.Ala5GlyfsTer?
ENST00000590625.5:c.13dup ENSP00000465705.1:p.Ala5GlyfsTer?
NM_000641.3:c.250dup NP_000632.1:p.Ala84GlyfsTer?
NM_001267718.1:c.13dup NP_001254647.1:p.Ala5GlyfsTer?
NM_000641.4:c.250dup MANE Select NP_000632.1:p.Ala84GlyfsTer?
NM_001267718.2:c.13dup NP_001254647.1:p.Ala5GlyfsTer?