Canonical Allele Identifier: CA2190489749

Gene: ARNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80591712_80591713delinsGA , CM000677.2:g.80591712_80591713delinsGA	GRCh38
NC_000015.9:g.80884053_80884054delinsGA , CM000677.1:g.80884053_80884054delinsGA	GRCh37
NC_000015.8:g.78671108_78671109delinsGA	NCBI36

Transcript Alleles

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