Canonical Allele Identifier: CA2541940458

Gene: ARNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80591731_80591750del , CM000677.2:g.80591731_80591750del	GRCh38
NC_000015.9:g.80884072_80884091del , CM000677.1:g.80884072_80884091del	GRCh37
NC_000015.8:g.78671127_78671146del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303329.9:c.2055+27_2055+46del MANE Select	ENSP00000307479.4:n.2055+27_2055+46del
ENST00000303329.8:c.2055+27_2055+46del	ENSP00000307479.4:n.2055+27_2055+46del
ENST00000527771.5:c.2022+27_2022+46del	ENSP00000453792.1:n.2022+27_2022+46del
ENST00000533983.5:c.2022+27_2022+46del	ENSP00000453651.1:n.2022+27_2022+46del
ENST00000610490.4:c.*353+27_*353+46del	ENSP00000483762.1:n.*353+27_*353+46del
ENST00000622346.4:c.2055+27_2055+46del	ENSP00000479393.1:n.2055+27_2055+46del
NM_014862.3:c.2055+27_2055+46del	NP_055677.3:n.2055+27_2055+46del
NM_014862.4:c.2055+27_2055+46del MANE Select	NP_055677.3:n.2055+27_2055+46del