Canonical Allele Identifier: CA353319637

Gene: IL17RD

Linked Data

• MyVariant Identifiers: chr3:g.57140165G>A (hg19) ; chr3:g.57106137G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.57106137G>A , CM000665.2:g.57106137G>A	GRCh38
NC_000003.11:g.57140165G>A , CM000665.1:g.57140165G>A	GRCh37
NC_000003.10:g.57115205G>A	NCBI36
NG_047158.1:g.69181C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000296318.12:c.568C>T MANE Select	ENSP00000296318.7:p.Gln190Ter
ENST00000296318.11:c.568C>T	ENSP00000296318.7:p.Gln190Ter
ENST00000320057.9:c.136C>T	ENSP00000322250.5:p.Gln46Ter
ENST00000463523.5:c.136C>T	ENSP00000417516.1:p.Gln46Ter
ENST00000467210.5:c.136C>T	ENSP00000418368.1:p.Gln46Ter
ENST00000469841.5:n.505C>T
NM_017563.3:c.568C>T	NP_060033.3:p.Gln190Ter
XM_005265238.3:c.484C>T	XP_005265295.1:p.Gln162Ter
XM_006713209.2:c.136C>T	XP_006713272.1:p.Gln46Ter
XM_011533849.1:c.496C>T	XP_011532151.1:p.Gln166Ter
XM_011533850.1:c.136C>T	XP_011532152.1:p.Gln46Ter
NM_001318864.1:c.136C>T	NP_001305793.1:p.Gln46Ter
NM_017563.4:c.568C>T	NP_060033.3:p.Gln190Ter
XM_005265238.4:c.484C>T	XP_005265295.1:p.Gln162Ter
XM_011533849.2:c.136C>T	XP_011532151.2:p.Gln46Ter
NM_017563.5:c.568C>T MANE Select	NP_060033.3:p.Gln190Ter
NM_001318864.2:c.136C>T	NP_001305793.1:p.Gln46Ter