Canonical Allele Identifier: CA13780405
Gene: IL17D HGNC NCBI

Linked Data

dbSNP Id: rs735539

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20705895A>G , CM000675.2:g.20705895A>G GRCh38
NC_000013.10:g.21280034A>G , CM000675.1:g.21280034A>G GRCh37
NC_000013.9:g.20178034A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000682841.1:c.290+1604A>G MANE Select ENSP00000508385.1:n.290+1604A>G
ENST00000304920.3:c.290+1604A>G ENSP00000302924.3:n.290+1604A>G
ENST00000468605.1:c.213+1604A>G
NM_138284.1:c.290+1604A>G NP_612141.1:n.290+1604A>G
XM_005266421.2:c.311+1604A>G XP_005266478.1:n.311+1604A>G
XM_011535116.1:c.311+1604A>G XP_011533418.1:n.311+1604A>G
XM_005266421.4:c.311+1604A>G XP_005266478.1:n.311+1604A>G
NM_001385221.1:c.311+1604A>G NP_001372150.1:n.311+1604A>G
NM_001385222.1:c.311+1604A>G NP_001372151.1:n.311+1604A>G
NM_001385223.1:c.290+1604A>G NP_001372152.1:n.290+1604A>G
NM_001385224.1:c.290+1604A>G MANE Select NP_001372153.1:n.290+1604A>G
NM_001385225.1:c.38+4240A>G NP_001372154.1:n.38+4240A>G
NM_138284.2:c.290+1604A>G NP_612141.1:n.290+1604A>G
NR_169590.1:n.229+2575A>G
NR_169591.1:n.581+1604A>G