Canonical Allele Identifier: CA2841799139

Gene: HTR3C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184060173dup , CM000665.2:g.184060173dup	GRCh38
NC_000003.11:g.183777961dup , CM000665.1:g.183777961dup	GRCh37
NC_000003.10:g.185260655dup	NCBI36
NG_012749.1:g.12127dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318351.2:c.1165dup MANE Select	ENSP00000322617.1:p.Ala389GlyfsTer?
ENST00000318351.1:c.1165dup	ENSP00000322617.1:p.Ala389GlyfsTer?
NM_130770.2:c.1165dup	NP_570126.2:p.Ala389GlyfsTer?
NM_130770.3:c.1165dup MANE Select	NP_570126.2:p.Ala389GlyfsTer?