Canonical Allele Identifier: CA353319622

Gene: IL17RD

Linked Data

• MyVariant Identifiers: chr3:g.57140161G>T (hg19) ; chr3:g.57106133G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.57106133G>T , CM000665.2:g.57106133G>T	GRCh38
NC_000003.11:g.57140161G>T , CM000665.1:g.57140161G>T	GRCh37
NC_000003.10:g.57115201G>T	NCBI36
NG_047158.1:g.69185C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000296318.12:c.572C>A MANE Select	ENSP00000296318.7:p.Pro191Gln
ENST00000296318.11:c.572C>A	ENSP00000296318.7:p.Pro191Gln
ENST00000320057.9:c.140C>A	ENSP00000322250.5:p.Pro47Gln
ENST00000463523.5:c.140C>A	ENSP00000417516.1:p.Pro47Gln
ENST00000467210.5:c.140C>A	ENSP00000418368.1:p.Pro47Gln
ENST00000469841.5:n.509C>A
NM_017563.3:c.572C>A	NP_060033.3:p.Pro191Gln
XM_005265238.3:c.488C>A	XP_005265295.1:p.Pro163Gln
XM_006713209.2:c.140C>A	XP_006713272.1:p.Pro47Gln
XM_011533849.1:c.500C>A	XP_011532151.1:p.Pro167Gln
XM_011533850.1:c.140C>A	XP_011532152.1:p.Pro47Gln
NM_001318864.1:c.140C>A	NP_001305793.1:p.Pro47Gln
NM_017563.4:c.572C>A	NP_060033.3:p.Pro191Gln
XM_005265238.4:c.488C>A	XP_005265295.1:p.Pro163Gln
XM_011533849.2:c.140C>A	XP_011532151.2:p.Pro47Gln
NM_017563.5:c.572C>A MANE Select	NP_060033.3:p.Pro191Gln
NM_001318864.2:c.140C>A	NP_001305793.1:p.Pro47Gln