Canonical Allele Identifier: CA2343387129

Gene: IL11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55368415C= , CM000681.2:g.55368415C=	GRCh38
NC_000019.9:g.55879783C= , CM000681.1:g.55879783C=	GRCh37
NC_000019.8:g.60571595C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000264563.7:c.268-44G= MANE Select	ENSP00000264563.1:n.268-44G=
ENST00000264563.6:c.268-44G=	ENSP00000264563.1:n.268-44G=
ENST00000585513.1:c.268-44G=	ENSP00000467355.1:n.268-44G=
ENST00000587093.1:c.31-44G=	ENSP00000468663.1:n.31-44G=
ENST00000590625.5:c.31-44G=	ENSP00000465705.1:n.31-44G=
NM_000641.3:c.268-44G=	NP_000632.1:n.268-44G=
NM_001267718.1:c.31-44G=	NP_001254647.1:n.31-44G=
NM_000641.4:c.268-44G= MANE Select	NP_000632.1:n.268-44G=
NM_001267718.2:c.31-44G=	NP_001254647.1:n.31-44G=