Canonical Allele Identifier: CA491688686

Gene: ARNT2

Linked Data

• COSMIC: COSM1608741
• MyVariant Identifiers: chr15:g.80883947del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.80591608del , CM000677.2:g.80591608del	GRCh38
NC_000015.9:g.80883949del , CM000677.1:g.80883949del	GRCh37
NC_000015.8:g.78671004del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303329.9:c.1959del MANE Select	ENSP00000307479.4:p.Ser654ArgfsTer?
ENST00000303329.8:c.1959del	ENSP00000307479.4:p.Ser654ArgfsTer?
ENST00000527771.5:c.1926del	ENSP00000453792.1:p.Ser643ArgfsTer?
ENST00000533983.5:c.1926del	ENSP00000453651.1:p.Ser643ArgfsTer?
ENST00000610490.4:c.*257del	ENSP00000483762.1:n.*257del
ENST00000622346.4:c.1959del	ENSP00000479393.1:p.Ser654ArgfsTer?
NM_014862.3:c.1959del	NP_055677.3:p.Ser654ArgfsTer?
NM_014862.4:c.1959del MANE Select	NP_055677.3:p.Ser654ArgfsTer?