Canonical Allele Identifier: CA2190457855

Gene: ARNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80451471_80451472delinsCT , CM000677.2:g.80451471_80451472delinsCT	GRCh38
NC_000015.9:g.80743812_80743813delinsCT , CM000677.1:g.80743812_80743813delinsCT	GRCh37
NC_000015.8:g.78530867_78530868delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303329.9:c.146+477_146+478delinsCT MANE Select	ENSP00000307479.4:n.146+477_146+478delinsCT
ENST00000303329.8:c.146+477_146+478delinsCT	ENSP00000307479.4:n.146+477_146+478delinsCT
ENST00000525103.1:c.-57+10093_-57+10094delinsCT	ENSP00000452961.1:n.-57+10093_-57+10094delinsCT
ENST00000527771.5:c.113+477_113+478delinsCT	ENSP00000453792.1:n.113+477_113+478delinsCT
ENST00000529181.1:n.312+477_312+478delinsCT
ENST00000533983.5:c.113+477_113+478delinsCT	ENSP00000453651.1:n.113+477_113+478delinsCT
ENST00000610490.4:c.146+477_146+478delinsCT	ENSP00000483762.1:n.146+477_146+478delinsCT
ENST00000622346.4:c.146+477_146+478delinsCT	ENSP00000479393.1:n.146+477_146+478delinsCT
NM_014862.3:c.146+477_146+478delinsCT	NP_055677.3:n.146+477_146+478delinsCT
NM_014862.4:c.146+477_146+478delinsCT MANE Select	NP_055677.3:n.146+477_146+478delinsCT