Canonical Allele Identifier: CA1830323935

Gene: IL33

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.6253571C= , CM000671.2:g.6253571C=	GRCh38
NC_000009.11:g.6253571C= , CM000671.1:g.6253571C=	GRCh37
NC_000009.10:g.6243571C=	NCBI36
NG_047209.1:g.43423C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682010.1:c.489C= MANE Select	ENSP00000507310.1:p.Tyr163=
ENST00000381434.7:c.489C=	ENSP00000370842.3:p.Tyr163=
ENST00000417746.6:c.111C=	ENSP00000394039.2:p.Tyr37=
ENST00000456383.3:c.363C=	ENSP00000414238.2:p.Tyr121=
ENST00000611532.4:c.363C=	ENSP00000478858.1:p.Tyr121=
NM_001199640.1:c.363C=	NP_001186569.1:p.Tyr121=
NM_001199641.1:c.111C=	NP_001186570.1:p.Tyr37=
NM_001314044.1:c.489C=	NP_001300973.1:p.Tyr163=
NM_001314045.1:c.489C=	NP_001300974.1:p.Tyr163=
NM_001314046.1:c.471C=	NP_001300975.1:p.Tyr157=
NM_001314047.1:c.471C=	NP_001300976.1:p.Tyr157=
NM_001314048.1:c.363C=	NP_001300977.1:p.Tyr121=
NM_033439.3:c.489C=	NP_254274.1:p.Tyr163=
XM_011518061.1:c.366C=	XP_011516363.1:p.Tyr122=
NM_001353802.1:c.366C=	NP_001340731.1:p.Tyr122=
XM_017015285.1:c.471C=	XP_016870774.1:p.Tyr157=
XR_001746614.1:n.153-25276G=
NM_001199640.2:c.363C=	NP_001186569.1:p.Tyr121=
NM_001314044.2:c.489C=	NP_001300973.1:p.Tyr163=
NM_001314045.2:c.489C=	NP_001300974.1:p.Tyr163=
NM_001314046.2:c.471C=	NP_001300975.1:p.Tyr157=
NM_001314047.2:c.471C=	NP_001300976.1:p.Tyr157=
NM_001314048.2:c.363C=	NP_001300977.1:p.Tyr121=
NM_001353802.2:c.366C=	NP_001340731.1:p.Tyr122=
NM_033439.4:c.489C= MANE Select	NP_254274.1:p.Tyr163=
NM_001199641.2:c.111C=	NP_001186570.1:p.Tyr37=