Canonical Allele Identifier: CA2587295016

Gene: IL11

Linked Data

• gnomAD v4: 19-55368499-GC-G

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000264563.7:c.250del MANE Select	ENSP00000264563.1:p.Ala84HisfsTer11
ENST00000264563.6:c.250del	ENSP00000264563.1:p.Ala84HisfsTer11
ENST00000585513.1:c.250del	ENSP00000467355.1:p.Ala84HisfsTer11
ENST00000587093.1:c.13del	ENSP00000468663.1:p.Ala5HisfsTer11
ENST00000590625.5:c.13del	ENSP00000465705.1:p.Ala5HisfsTer11
NM_000641.3:c.250del	NP_000632.1:p.Ala84HisfsTer11
NM_001267718.1:c.13del	NP_001254647.1:p.Ala5HisfsTer11
NM_000641.4:c.250del MANE Select	NP_000632.1:p.Ala84HisfsTer11
NM_001267718.2:c.13del	NP_001254647.1:p.Ala5HisfsTer11