Canonical Allele Identifier: CA2045533045

Gene: TPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71994402_71994403delinsCT , CM000674.2:g.71994402_71994403delinsCT	GRCh38
NC_000012.11:g.72388182_72388183delinsCT , CM000674.1:g.72388182_72388183delinsCT	GRCh37
NC_000012.10:g.70674449_70674450delinsCT	NCBI36
NG_008279.1:g.60557_60558delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333850.4:c.942-37_942-36delinsCT MANE Select	ENSP00000329093.3:n.942-37_942-36delinsCT
ENST00000333850.3:c.942-37_942-36delinsCT	ENSP00000329093.3:n.942-37_942-36delinsCT
NM_173353.3:c.942-37_942-36delinsCT	NP_775489.2:n.942-37_942-36delinsCT
XM_011537899.1:c.348-37_348-36delinsCT	XP_011536201.1:n.348-37_348-36delinsCT
NM_173353.4:c.942-37_942-36delinsCT MANE Select	NP_775489.2:n.942-37_942-36delinsCT