Canonical Allele Identifier: CA74987423

Gene: IL17RD

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_017563.5:c.1403C>G MANE Select	NP_060033.3:p.Ser468Trp
ENST00000296318.12:c.1403C>G MANE Select	ENSP00000296318.7:p.Ser468Trp
NM_001318864.1:c.971C>G	NP_001305793.1:p.Ser324Trp
NM_001318864.2:c.971C>G	NP_001305793.1:p.Ser324Trp
NM_017563.3:c.1403C>G	NP_060033.3:p.Ser468Trp
NM_017563.4:c.1403C>G	NP_060033.3:p.Ser468Trp
ENST00000296318.11:c.1403C>G	ENSP00000296318.7:p.Ser468Trp
ENST00000320057.9:c.971C>G	ENSP00000322250.5:p.Ser324Trp
ENST00000463523.5:c.971C>G	ENSP00000417516.1:p.Ser324Trp
ENST00000469841.5:n.1340C>G
XM_005265238.3:c.1319C>G	XP_005265295.1:p.Ser440Trp
XM_005265238.4:c.1319C>G	XP_005265295.1:p.Ser440Trp
XM_006713209.2:c.971C>G	XP_006713272.1:p.Ser324Trp
XM_011533849.1:c.1331C>G	XP_011532151.1:p.Ser444Trp
XM_011533849.2:c.971C>G	XP_011532151.2:p.Ser324Trp
XM_011533850.1:c.971C>G	XP_011532152.1:p.Ser324Trp