Canonical Allele Identifier: CA434141124

Gene: IL17RD

Linked Data

• gnomAD v4: 3-57106135-C-T
• MyVariant Identifiers: chr3:g.57140163C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.57106135C>T , CM000665.2:g.57106135C>T	GRCh38
NC_000003.11:g.57140163C>T , CM000665.1:g.57140163C>T	GRCh37
NC_000003.10:g.57115203C>T	NCBI36
NG_047158.1:g.69183G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000296318.12:c.570G>A MANE Select	ENSP00000296318.7:p.Gln190=
ENST00000296318.11:c.570G>A	ENSP00000296318.7:p.Gln190=
ENST00000320057.9:c.138G>A	ENSP00000322250.5:p.Gln46=
ENST00000463523.5:c.138G>A	ENSP00000417516.1:p.Gln46=
ENST00000467210.5:c.138G>A	ENSP00000418368.1:p.Gln46=
ENST00000469841.5:n.507G>A
NM_017563.3:c.570G>A	NP_060033.3:p.Gln190=
XM_005265238.3:c.486G>A	XP_005265295.1:p.Gln162=
XM_006713209.2:c.138G>A	XP_006713272.1:p.Gln46=
XM_011533849.1:c.498G>A	XP_011532151.1:p.Gln166=
XM_011533850.1:c.138G>A	XP_011532152.1:p.Gln46=
NM_001318864.1:c.138G>A	NP_001305793.1:p.Gln46=
NM_017563.4:c.570G>A	NP_060033.3:p.Gln190=
XM_005265238.4:c.486G>A	XP_005265295.1:p.Gln162=
XM_011533849.2:c.138G>A	XP_011532151.2:p.Gln46=
NM_017563.5:c.570G>A MANE Select	NP_060033.3:p.Gln190=
NM_001318864.2:c.138G>A	NP_001305793.1:p.Gln46=