Canonical Allele Identifier: CA2629889105

Gene: ARNT2

Linked Data

• gnomAD v4: 15-80591824-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80591827del , CM000677.2:g.80591827del	GRCh38
NC_000015.9:g.80884168del , CM000677.1:g.80884168del	GRCh37
NC_000015.8:g.78671223del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303329.9:c.2055+123del MANE Select	ENSP00000307479.4:n.2055+123del
ENST00000303329.8:c.2055+123del	ENSP00000307479.4:n.2055+123del
ENST00000527771.5:c.2022+123del	ENSP00000453792.1:n.2022+123del
ENST00000533983.5:c.2022+123del	ENSP00000453651.1:n.2022+123del
ENST00000610490.4:c.*353+123del	ENSP00000483762.1:n.*353+123del
ENST00000622346.4:c.2055+123del	ENSP00000479393.1:n.2055+123del
NM_014862.3:c.2055+123del	NP_055677.3:n.2055+123del
NM_014862.4:c.2055+123del MANE Select	NP_055677.3:n.2055+123del