Canonical Allele Identifier: CA1830323880

Gene: IL33

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6253484T= , CM000671.2:g.6253484T=	GRCh38
NC_000009.11:g.6253484T= , CM000671.1:g.6253484T=	GRCh37
NC_000009.10:g.6243484T=	NCBI36
NG_047209.1:g.43336T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682010.1:c.470-68T= MANE Select	ENSP00000507310.1:n.470-68T=
ENST00000381434.7:c.470-68T=	ENSP00000370842.3:n.470-68T=
ENST00000417746.6:c.92-68T=	ENSP00000394039.2:n.92-68T=
ENST00000456383.3:c.344-68T=	ENSP00000414238.2:n.344-68T=
ENST00000611532.4:c.344-68T=	ENSP00000478858.1:n.344-68T=
NM_001199640.1:c.344-68T=	NP_001186569.1:n.344-68T=
NM_001199641.1:c.92-68T=	NP_001186570.1:n.92-68T=
NM_001314044.1:c.470-68T=	NP_001300973.1:n.470-68T=
NM_001314045.1:c.470-68T=	NP_001300974.1:n.470-68T=
NM_001314046.1:c.452-68T=	NP_001300975.1:n.452-68T=
NM_001314047.1:c.452-68T=	NP_001300976.1:n.452-68T=
NM_001314048.1:c.344-68T=	NP_001300977.1:n.344-68T=
NM_033439.3:c.470-68T=	NP_254274.1:n.470-68T=
XM_011518061.1:c.347-68T=	XP_011516363.1:n.347-68T=
NM_001353802.1:c.347-68T=	NP_001340731.1:n.347-68T=
XM_017015285.1:c.452-68T=	XP_016870774.1:n.452-68T=
XR_001746614.1:n.153-25189A=
NM_001199640.2:c.344-68T=	NP_001186569.1:n.344-68T=
NM_001314044.2:c.470-68T=	NP_001300973.1:n.470-68T=
NM_001314045.2:c.470-68T=	NP_001300974.1:n.470-68T=
NM_001314046.2:c.452-68T=	NP_001300975.1:n.452-68T=
NM_001314047.2:c.452-68T=	NP_001300976.1:n.452-68T=
NM_001314048.2:c.344-68T=	NP_001300977.1:n.344-68T=
NM_001353802.2:c.347-68T=	NP_001340731.1:n.347-68T=
NM_033439.4:c.470-68T= MANE Select	NP_254274.1:n.470-68T=
NM_001199641.2:c.92-68T=	NP_001186570.1:n.92-68T=