Canonical Allele Identifier: CA353319673

Gene: IL17RD

Linked Data

• MyVariant Identifiers: chr3:g.57140175G>C (hg19) ; chr3:g.57106147G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.57106147G>C , CM000665.2:g.57106147G>C	GRCh38
NC_000003.11:g.57140175G>C , CM000665.1:g.57140175G>C	GRCh37
NC_000003.10:g.57115215G>C	NCBI36
NG_047158.1:g.69171C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000296318.12:c.558C>G MANE Select	ENSP00000296318.7:p.Asp186Glu
ENST00000296318.11:c.558C>G	ENSP00000296318.7:p.Asp186Glu
ENST00000320057.9:c.126C>G	ENSP00000322250.5:p.Asp42Glu
ENST00000463523.5:c.126C>G	ENSP00000417516.1:p.Asp42Glu
ENST00000467210.5:c.126C>G	ENSP00000418368.1:p.Asp42Glu
ENST00000469841.5:n.495C>G
NM_017563.3:c.558C>G	NP_060033.3:p.Asp186Glu
XM_005265238.3:c.474C>G	XP_005265295.1:p.Asp158Glu
XM_006713209.2:c.126C>G	XP_006713272.1:p.Asp42Glu
XM_011533849.1:c.486C>G	XP_011532151.1:p.Asp162Glu
XM_011533850.1:c.126C>G	XP_011532152.1:p.Asp42Glu
NM_001318864.1:c.126C>G	NP_001305793.1:p.Asp42Glu
NM_017563.4:c.558C>G	NP_060033.3:p.Asp186Glu
XM_005265238.4:c.474C>G	XP_005265295.1:p.Asp158Glu
XM_011533849.2:c.126C>G	XP_011532151.2:p.Asp42Glu
NM_017563.5:c.558C>G MANE Select	NP_060033.3:p.Asp186Glu
NM_001318864.2:c.126C>G	NP_001305793.1:p.Asp42Glu