Canonical Allele Identifier: CA1845645508

Gene: IL11RA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34652246G= , CM000671.2:g.34652246G=	GRCh38
NC_000009.11:g.34652243G= , CM000671.1:g.34652243G=	GRCh37
NC_000009.10:g.34642243G=	NCBI36
NG_009029.1:g.10609G=
NG_028966.1:g.5062G=
NG_009029.2:g.10658G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000553620.6:c.-1+13G=	ENSP00000452207.2:n.-1+13G=
ENST00000555003.6:c.-1+13G=	ENSP00000450565.2:n.-1+13G=
ENST00000556531.6:c.-1+13G=	ENSP00000451447.2:n.-1+13G=
ENST00000684861.1:n.53+13G=
ENST00000690286.1:c.-86+13G=	ENSP00000509204.1:n.-86+13G=
ENST00000691183.1:c.*2336+189G=	ENSP00000509954.1:n.*2336+189G=
ENST00000692291.1:n.48+13G=
ENST00000692530.1:n.61+13G=
ENST00000441545.7:c.-1+13G= MANE Select	ENSP00000394391.3:n.-1+13G=
ENST00000441545.6:c.-1+13G=	ENSP00000394391.2:n.-1+13G=
ENST00000553620.5:c.-1+13G=	ENSP00000452207.1:n.-1+13G=
ENST00000555003.5:c.-1+189G=	ENSP00000450565.1:n.-1+189G=
ENST00000555247.5:c.-1+13G=	ENSP00000450707.1:n.-1+13G=
ENST00000556278.1:c.433-2972G=	ENSP00000451792.1:n.433-2972G=
NM_001142784.2:c.-1+13G=	NP_001136256.1:n.-1+13G=
NM_001142784.3:c.-1+13G= MANE Select	NP_001136256.1:n.-1+13G=