Canonical Allele Identifier: CA1367040395

Gene: IL17RD

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.57098300G= , CM000665.2:g.57098300G=	GRCh38
NC_000003.11:g.57132328G= , CM000665.1:g.57132328G=	GRCh37
NC_000003.10:g.57107368G=	NCBI36
NG_047158.1:g.77018C=

Transcript Alleles

HGVS	Amino-acid Change
NM_017563.5:c.1403C= MANE Select	NP_060033.3:p.Ser468=
ENST00000296318.12:c.1403C= MANE Select	ENSP00000296318.7:p.Ser468=
NM_001318864.1:c.971C=	NP_001305793.1:p.Ser324=
NM_001318864.2:c.971C=	NP_001305793.1:p.Ser324=
NM_017563.3:c.1403C=	NP_060033.3:p.Ser468=
NM_017563.4:c.1403C=	NP_060033.3:p.Ser468=
ENST00000296318.11:c.1403C=	ENSP00000296318.7:p.Ser468=
ENST00000320057.9:c.971C=	ENSP00000322250.5:p.Ser324=
ENST00000463523.5:c.971C=	ENSP00000417516.1:p.Ser324=
ENST00000469841.5:n.1340C=
XM_005265238.3:c.1319C=	XP_005265295.1:p.Ser440=
XM_005265238.4:c.1319C=	XP_005265295.1:p.Ser440=
XM_006713209.2:c.971C=	XP_006713272.1:p.Ser324=
XM_011533849.1:c.1331C=	XP_011532151.1:p.Ser444=
XM_011533849.2:c.971C=	XP_011532151.2:p.Ser324=
XM_011533850.1:c.971C=	XP_011532152.1:p.Ser324=