Canonical Allele Identifier: CA359771701

Gene: IL31RA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.55910592C>T , CM000667.2:g.55910592C>T	GRCh38
NC_000005.9:g.55206420C>T , CM000667.1:g.55206420C>T	GRCh37
NC_000005.8:g.55242177C>T	NCBI36
NG_029436.1:g.64214C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_139017.7:c.1562C>T MANE Select	NP_620586.3:p.Ser521Phe
ENST00000652347.2:c.1562C>T MANE Select	ENSP00000498630.1:p.Ser521Phe
NM_001242636.1:c.1505C>T	NP_001229565.1:p.Ser502Phe
NM_001242636.2:c.1505C>T	NP_001229565.1:p.Ser502Phe
NM_001242637.1:c.1562C>T	NP_001229566.1:p.Ser521Phe
NM_001242637.2:c.1562C>T	NP_001229566.1:p.Ser521Phe
NM_001242638.1:c.1505C>T	NP_001229567.1:p.Ser502Phe
NM_001242638.2:c.1505C>T	NP_001229567.1:p.Ser502Phe
NM_001242639.1:c.1136C>T	NP_001229568.1:p.Ser379Phe
NM_001242639.2:c.1136C>T	NP_001229568.1:p.Ser379Phe
NM_139017.5:c.1562C>T	NP_620586.3:p.Ser521Phe
NM_139017.6:c.1562C>T	NP_620586.3:p.Ser521Phe
ENST00000297015.7:c.1505C>T	ENSP00000297015.4:p.Ser502Phe
ENST00000354961.8:c.1505C>T	ENSP00000347047.4:p.Ser502Phe
ENST00000359040.10:c.1562C>T	ENSP00000351935.5:p.Ser521Phe
ENST00000359040.9:c.1562C>T	ENSP00000351935.5:p.Ser521Phe
ENST00000396834.5:c.1505C>T	ENSP00000380046.1:p.Ser502Phe
ENST00000396834.6:c.*1713C>T	ENSP00000380046.2:n.*1713C>T
ENST00000447346.6:c.1562C>T	ENSP00000415900.2:p.Ser521Phe
ENST00000490985.5:c.1136C>T	ENSP00000427533.1:p.Ser379Phe
ENST00000652039.1:c.1490C>T	ENSP00000498914.1:p.Ser497Phe
ENST00000652347.1:c.1562C>T	ENSP00000498630.1:p.Ser521Phe
XM_011543142.1:c.1466C>T	XP_011541444.1:p.Ser489Phe
XM_011543142.2:c.1466C>T	XP_011541444.1:p.Ser489Phe
XM_011543143.1:c.1505C>T	XP_011541445.1:p.Ser502Phe
XM_011543143.2:c.1505C>T	XP_011541445.1:p.Ser502Phe
XM_011543144.1:c.1136C>T	XP_011541446.1:p.Ser379Phe
XM_011543144.2:c.1136C>T	XP_011541446.1:p.Ser379Phe
XM_011543145.1:c.1052C>T	XP_011541447.1:p.Ser351Phe
XM_011543145.2:c.1052C>T	XP_011541447.1:p.Ser351Phe