Canonical Allele Identifier: CA2343387133

Gene: IL11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.55368428G= , CM000681.2:g.55368428G=	GRCh38
NC_000019.9:g.55879796G= , CM000681.1:g.55879796G=	GRCh37
NC_000019.8:g.60571608G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000264563.7:c.267+55C= MANE Select	ENSP00000264563.1:n.267+55C=
ENST00000264563.6:c.267+55C=	ENSP00000264563.1:n.267+55C=
ENST00000585513.1:c.267+55C=	ENSP00000467355.1:n.267+55C=
ENST00000587093.1:c.30+55C=	ENSP00000468663.1:n.30+55C=
ENST00000590625.5:c.30+55C=	ENSP00000465705.1:n.30+55C=
NM_000641.3:c.267+55C=	NP_000632.1:n.267+55C=
NM_001267718.1:c.30+55C=	NP_001254647.1:n.30+55C=
NM_000641.4:c.267+55C= MANE Select	NP_000632.1:n.267+55C=
NM_001267718.2:c.30+55C=	NP_001254647.1:n.30+55C=