Canonical Allele Identifier: CA353319635

Gene: IL17RD

Linked Data

• MyVariant Identifiers: chr3:g.57140164T>G (hg19) ; chr3:g.57106136T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.57106136T>G , CM000665.2:g.57106136T>G	GRCh38
NC_000003.11:g.57140164T>G , CM000665.1:g.57140164T>G	GRCh37
NC_000003.10:g.57115204T>G	NCBI36
NG_047158.1:g.69182A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000296318.12:c.569A>C MANE Select	ENSP00000296318.7:p.Gln190Pro
ENST00000296318.11:c.569A>C	ENSP00000296318.7:p.Gln190Pro
ENST00000320057.9:c.137A>C	ENSP00000322250.5:p.Gln46Pro
ENST00000463523.5:c.137A>C	ENSP00000417516.1:p.Gln46Pro
ENST00000467210.5:c.137A>C	ENSP00000418368.1:p.Gln46Pro
ENST00000469841.5:n.506A>C
NM_017563.3:c.569A>C	NP_060033.3:p.Gln190Pro
XM_005265238.3:c.485A>C	XP_005265295.1:p.Gln162Pro
XM_006713209.2:c.137A>C	XP_006713272.1:p.Gln46Pro
XM_011533849.1:c.497A>C	XP_011532151.1:p.Gln166Pro
XM_011533850.1:c.137A>C	XP_011532152.1:p.Gln46Pro
NM_001318864.1:c.137A>C	NP_001305793.1:p.Gln46Pro
NM_017563.4:c.569A>C	NP_060033.3:p.Gln190Pro
XM_005265238.4:c.485A>C	XP_005265295.1:p.Gln162Pro
XM_011533849.2:c.137A>C	XP_011532151.2:p.Gln46Pro
NM_017563.5:c.569A>C MANE Select	NP_060033.3:p.Gln190Pro
NM_001318864.2:c.137A>C	NP_001305793.1:p.Gln46Pro