Canonical Allele Identifier: CA1547698103

Gene: IL31RA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55916602A= , CM000667.2:g.55916602A=	GRCh38
NC_000005.9:g.55212430A= , CM000667.1:g.55212430A=	GRCh37
NC_000005.8:g.55248187A=	NCBI36
NG_029436.1:g.70224A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652347.2:c.1819-42A= MANE Select	ENSP00000498630.1:n.1819-42A=
ENST00000359040.10:c.1819-42A=	ENSP00000351935.5:n.1819-42A=
ENST00000396834.6:c.*1970-42A=	ENSP00000380046.2:n.*1970-42A=
ENST00000652347.1:c.1819-42A=	ENSP00000498630.1:n.1819-42A=
ENST00000297015.7:c.1762-42A=	ENSP00000297015.4:n.1762-42A=
ENST00000354961.8:c.1762-42A=	ENSP00000347047.4:n.1762-42A=
ENST00000359040.9:c.1819-42A=	ENSP00000351935.5:n.1819-42A=
ENST00000396834.5:c.1762-42A=	ENSP00000380046.1:n.1762-42A=
ENST00000447346.6:c.1819-42A=	ENSP00000415900.2:n.1819-42A=
ENST00000490985.5:c.1393-42A=	ENSP00000427533.1:n.1393-42A=
NM_001242636.1:c.1762-42A=	NP_001229565.1:n.1762-42A=
NM_001242637.1:c.1819-42A=	NP_001229566.1:n.1819-42A=
NM_001242638.1:c.1762-42A=	NP_001229567.1:n.1762-42A=
NM_001242639.1:c.1393-42A=	NP_001229568.1:n.1393-42A=
NM_139017.5:c.1819-42A=	NP_620586.3:n.1819-42A=
XM_011543142.1:c.1723-42A=	XP_011541444.1:n.1723-42A=
XM_011543143.1:c.1762-42A=	XP_011541445.1:n.1762-42A=
XM_011543144.1:c.1393-42A=	XP_011541446.1:n.1393-42A=
XM_011543145.1:c.1309-42A=	XP_011541447.1:n.1309-42A=
XM_011543142.2:c.1723-42A=	XP_011541444.1:n.1723-42A=
XM_011543143.2:c.1762-42A=	XP_011541445.1:n.1762-42A=
XM_011543144.2:c.1393-42A=	XP_011541446.1:n.1393-42A=
XM_011543145.2:c.1309-42A=	XP_011541447.1:n.1309-42A=
NM_001242637.2:c.1819-42A=	NP_001229566.1:n.1819-42A=
NM_001242638.2:c.1762-42A=	NP_001229567.1:n.1762-42A=
NM_139017.6:c.1819-42A=	NP_620586.3:n.1819-42A=
NM_001242636.2:c.1762-42A=	NP_001229565.1:n.1762-42A=
NM_001242639.2:c.1393-42A=	NP_001229568.1:n.1393-42A=
NM_139017.7:c.1819-42A= MANE Select	NP_620586.3:n.1819-42A=