Canonical Allele Identifier: CA2077411590

Gene: IL17D

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.20705964C= , CM000675.2:g.20705964C=	GRCh38
NC_000013.10:g.21280103C= , CM000675.1:g.21280103C=	GRCh37
NC_000013.9:g.20178103C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682841.1:c.290+1673C= MANE Select	ENSP00000508385.1:n.290+1673C=
ENST00000304920.3:c.290+1673C=	ENSP00000302924.3:n.290+1673C=
ENST00000468605.1:c.213+1673C=
NM_138284.1:c.290+1673C=	NP_612141.1:n.290+1673C=
XM_005266421.2:c.311+1673C=	XP_005266478.1:n.311+1673C=
XM_011535116.1:c.311+1673C=	XP_011533418.1:n.311+1673C=
XM_005266421.4:c.311+1673C=	XP_005266478.1:n.311+1673C=
NM_001385221.1:c.311+1673C=	NP_001372150.1:n.311+1673C=
NM_001385222.1:c.311+1673C=	NP_001372151.1:n.311+1673C=
NM_001385223.1:c.290+1673C=	NP_001372152.1:n.290+1673C=
NM_001385224.1:c.290+1673C= MANE Select	NP_001372153.1:n.290+1673C=
NM_001385225.1:c.38+4309C=	NP_001372154.1:n.38+4309C=
NM_138284.2:c.290+1673C=	NP_612141.1:n.290+1673C=
NR_169590.1:n.229+2644C=
NR_169591.1:n.581+1673C=