Canonical Allele Identifier: CA353319644

Gene: IL17RD

Linked Data

• MyVariant Identifiers: chr3:g.57140166T>G (hg19) ; chr3:g.57106138T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.57106138T>G , CM000665.2:g.57106138T>G	GRCh38
NC_000003.11:g.57140166T>G , CM000665.1:g.57140166T>G	GRCh37
NC_000003.10:g.57115206T>G	NCBI36
NG_047158.1:g.69180A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000296318.12:c.567A>C MANE Select	ENSP00000296318.7:p.Leu189Phe
ENST00000296318.11:c.567A>C	ENSP00000296318.7:p.Leu189Phe
ENST00000320057.9:c.135A>C	ENSP00000322250.5:p.Leu45Phe
ENST00000463523.5:c.135A>C	ENSP00000417516.1:p.Leu45Phe
ENST00000467210.5:c.135A>C	ENSP00000418368.1:p.Leu45Phe
ENST00000469841.5:n.504A>C
NM_017563.3:c.567A>C	NP_060033.3:p.Leu189Phe
XM_005265238.3:c.483A>C	XP_005265295.1:p.Leu161Phe
XM_006713209.2:c.135A>C	XP_006713272.1:p.Leu45Phe
XM_011533849.1:c.495A>C	XP_011532151.1:p.Leu165Phe
XM_011533850.1:c.135A>C	XP_011532152.1:p.Leu45Phe
NM_001318864.1:c.135A>C	NP_001305793.1:p.Leu45Phe
NM_017563.4:c.567A>C	NP_060033.3:p.Leu189Phe
XM_005265238.4:c.483A>C	XP_005265295.1:p.Leu161Phe
XM_011533849.2:c.135A>C	XP_011532151.2:p.Leu45Phe
NM_017563.5:c.567A>C MANE Select	NP_060033.3:p.Leu189Phe
NM_001318864.2:c.135A>C	NP_001305793.1:p.Leu45Phe