Canonical Allele Identifier: CA2629889078

Gene: ARNT2

Linked Data

• gnomAD v4: 15-80591800-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80591802del , CM000677.2:g.80591802del	GRCh38
NC_000015.9:g.80884143del , CM000677.1:g.80884143del	GRCh37
NC_000015.8:g.78671198del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303329.9:c.2055+98del MANE Select	ENSP00000307479.4:n.2055+98del
ENST00000303329.8:c.2055+98del	ENSP00000307479.4:n.2055+98del
ENST00000527771.5:c.2022+98del	ENSP00000453792.1:n.2022+98del
ENST00000533983.5:c.2022+98del	ENSP00000453651.1:n.2022+98del
ENST00000610490.4:c.*353+98del	ENSP00000483762.1:n.*353+98del
ENST00000622346.4:c.2055+98del	ENSP00000479393.1:n.2055+98del
NM_014862.3:c.2055+98del	NP_055677.3:n.2055+98del
NM_014862.4:c.2055+98del MANE Select	NP_055677.3:n.2055+98del