Canonical Allele Identifier: CA2190489834

Gene: ARNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80591775_80591776delinsCT , CM000677.2:g.80591775_80591776delinsCT	GRCh38
NC_000015.9:g.80884116_80884117delinsCT , CM000677.1:g.80884116_80884117delinsCT	GRCh37
NC_000015.8:g.78671171_78671172delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303329.9:c.2055+71_2055+72delinsCT MANE Select	ENSP00000307479.4:n.2055+71_2055+72delinsCT
ENST00000303329.8:c.2055+71_2055+72delinsCT	ENSP00000307479.4:n.2055+71_2055+72delinsCT
ENST00000527771.5:c.2022+71_2022+72delinsCT	ENSP00000453792.1:n.2022+71_2022+72delinsCT
ENST00000533983.5:c.2022+71_2022+72delinsCT	ENSP00000453651.1:n.2022+71_2022+72delinsCT
ENST00000610490.4:c.*353+71_*353+72delinsCT	ENSP00000483762.1:n.*353+71_*353+72delinsCT
ENST00000622346.4:c.2055+71_2055+72delinsCT	ENSP00000479393.1:n.2055+71_2055+72delinsCT
NM_014862.3:c.2055+71_2055+72delinsCT	NP_055677.3:n.2055+71_2055+72delinsCT
NM_014862.4:c.2055+71_2055+72delinsCT MANE Select	NP_055677.3:n.2055+71_2055+72delinsCT