Canonical Allele Identifier: CA353319656

Gene: IL17RD

Linked Data

• MyVariant Identifiers: chr3:g.57140170A>C (hg19) ; chr3:g.57106142A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.57106142A>C , CM000665.2:g.57106142A>C	GRCh38
NC_000003.11:g.57140170A>C , CM000665.1:g.57140170A>C	GRCh37
NC_000003.10:g.57115210A>C	NCBI36
NG_047158.1:g.69176T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000296318.12:c.563T>G MANE Select	ENSP00000296318.7:p.Leu188Trp
ENST00000296318.11:c.563T>G	ENSP00000296318.7:p.Leu188Trp
ENST00000320057.9:c.131T>G	ENSP00000322250.5:p.Leu44Trp
ENST00000463523.5:c.131T>G	ENSP00000417516.1:p.Leu44Trp
ENST00000467210.5:c.131T>G	ENSP00000418368.1:p.Leu44Trp
ENST00000469841.5:n.500T>G
NM_017563.3:c.563T>G	NP_060033.3:p.Leu188Trp
XM_005265238.3:c.479T>G	XP_005265295.1:p.Leu160Trp
XM_006713209.2:c.131T>G	XP_006713272.1:p.Leu44Trp
XM_011533849.1:c.491T>G	XP_011532151.1:p.Leu164Trp
XM_011533850.1:c.131T>G	XP_011532152.1:p.Leu44Trp
NM_001318864.1:c.131T>G	NP_001305793.1:p.Leu44Trp
NM_017563.4:c.563T>G	NP_060033.3:p.Leu188Trp
XM_005265238.4:c.479T>G	XP_005265295.1:p.Leu160Trp
XM_011533849.2:c.131T>G	XP_011532151.2:p.Leu44Trp
NM_017563.5:c.563T>G MANE Select	NP_060033.3:p.Leu188Trp
NM_001318864.2:c.131T>G	NP_001305793.1:p.Leu44Trp