Canonical Allele Identifier: CA3271052

Gene: IL31RA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55916968G>A , CM000667.2:g.55916968G>A	GRCh38
NC_000005.9:g.55212796G>A , CM000667.1:g.55212796G>A	GRCh37
NC_000005.8:g.55248553G>A	NCBI36
NG_029436.1:g.70590G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_139017.7:c.2143G>A MANE Select	NP_620586.3:p.Ala715Thr
ENST00000652347.2:c.2143G>A MANE Select	ENSP00000498630.1:p.Ala715Thr
NM_001242636.1:c.2086G>A	NP_001229565.1:p.Ala696Thr
NM_001242636.2:c.2086G>A	NP_001229565.1:p.Ala696Thr
NM_001242637.1:c.2009+134G>A	NP_001229566.1:n.2009+134G>A
NM_001242637.2:c.2009+134G>A	NP_001229566.1:n.2009+134G>A
NM_001242638.1:c.1952+134G>A	NP_001229567.1:n.1952+134G>A
NM_001242638.2:c.1952+134G>A	NP_001229567.1:n.1952+134G>A
NM_001242639.1:c.1717G>A	NP_001229568.1:p.Ala573Thr
NM_001242639.2:c.1717G>A	NP_001229568.1:p.Ala573Thr
NM_139017.5:c.2143G>A	NP_620586.3:p.Ala715Thr
NM_139017.6:c.2143G>A	NP_620586.3:p.Ala715Thr
ENST00000297015.7:c.2086G>A	ENSP00000297015.4:p.Ala696Thr
ENST00000354961.8:c.1952+134G>A	ENSP00000347047.4:n.1952+134G>A
ENST00000359040.10:c.2009+134G>A	ENSP00000351935.5:n.2009+134G>A
ENST00000359040.9:c.2009+134G>A	ENSP00000351935.5:n.2009+134G>A
ENST00000396834.5:c.1952+134G>A	ENSP00000380046.1:n.1952+134G>A
ENST00000396834.6:c.*2160+134G>A	ENSP00000380046.2:n.*2160+134G>A
ENST00000447346.6:c.2143G>A	ENSP00000415900.2:p.Ala715Thr
ENST00000490985.5:c.1717G>A	ENSP00000427533.1:p.Ala573Thr
ENST00000652347.1:c.2143G>A	ENSP00000498630.1:p.Ala715Thr
XM_011543142.1:c.2047G>A	XP_011541444.1:p.Ala683Thr
XM_011543142.2:c.2047G>A	XP_011541444.1:p.Ala683Thr
XM_011543143.1:c.1952+134G>A	XP_011541445.1:n.1952+134G>A
XM_011543143.2:c.1952+134G>A	XP_011541445.1:n.1952+134G>A
XM_011543144.1:c.1717G>A	XP_011541446.1:p.Ala573Thr
XM_011543144.2:c.1717G>A	XP_011541446.1:p.Ala573Thr
XM_011543145.1:c.1633G>A	XP_011541447.1:p.Ala545Thr
XM_011543145.2:c.1633G>A	XP_011541447.1:p.Ala545Thr