Canonical Allele Identifier: CA1845655346

Gene: IL11RA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34660867C= , CM000671.2:g.34660867C=	GRCh38
NC_000009.11:g.34660864C= , CM000671.1:g.34660864C=	GRCh37
NC_000009.10:g.34650864C=	NCBI36
NG_028966.1:g.13683C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001142784.3:c.1183C= MANE Select	NP_001136256.1:p.Arg395=
ENST00000441545.7:c.1183C= MANE Select	ENSP00000394391.3:p.Arg395=
NM_001142784.2:c.1183C=	NP_001136256.1:p.Arg395=
NR_052010.1:n.1286C=
NR_052010.2:n.1270C=
ENST00000318041.13:c.1183C=	ENSP00000326500.8:p.Arg395=
ENST00000441545.6:c.1183C=	ENSP00000394391.2:p.Arg395=
ENST00000466082.1:c.296C=
ENST00000466082.2:c.1233C=	ENSP00000432263.2:n.1233C=
ENST00000478308.2:n.1654C=
ENST00000553620.6:c.952C=	ENSP00000452207.2:p.Arg318=
ENST00000555003.5:c.1183C=	ENSP00000450565.1:p.Arg395=
ENST00000555003.6:c.1195C=	ENSP00000450565.2:p.Arg399=
ENST00000555247.5:c.*957C=	ENSP00000450707.1:n.*957C=
ENST00000555981.6:c.1183C=	ENSP00000450640.2:p.Arg395=
ENST00000556531.6:c.1169+267C=	ENSP00000451447.2:n.1169+267C=
ENST00000557298.5:c.*806C=	ENSP00000451553.1:n.*806C=
ENST00000684861.1:n.1776C=
ENST00000685278.1:n.902C=
ENST00000685430.1:c.1264C=	ENSP00000510344.1:n.1264C=
ENST00000685662.1:n.1317C=
ENST00000685768.1:n.1844C=
ENST00000686794.1:n.879C=
ENST00000687192.1:n.1068C=
ENST00000687770.1:n.2377C=
ENST00000690286.1:c.1183C=	ENSP00000509204.1:p.Arg395=
ENST00000691183.1:c.*3568C=	ENSP00000509954.1:n.*3568C=
ENST00000692291.1:n.1484C=
ENST00000692530.1:n.1550C=
ENST00000692788.1:c.*1210C=	ENSP00000510222.1:n.*1210C=