Canonical Allele Identifier: CA2045515511

Gene: TPH2

Linked Data

• dbSNP Id: rs1871254843

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71948405_71948406del , CM000674.2:g.71948405_71948406del	GRCh38
NC_000012.11:g.72342185_72342186del , CM000674.1:g.72342185_72342186del	GRCh37
NC_000012.10:g.70628452_70628453del	NCBI36
NG_008279.1:g.14560_14561del

Transcript Alleles

HGVS	Amino-acid change
ENST00000333850.4:c.541-1183_541-1182del MANE Select	ENSP00000329093.3:n.541-1183_541-1182del
ENST00000333850.3:c.541-1183_541-1182del	ENSP00000329093.3:n.541-1183_541-1182del
ENST00000546576.1:n.551-1183_551-1182del
NM_173353.3:c.541-1183_541-1182del	NP_775489.2:n.541-1183_541-1182del
XM_011537899.1:c.-55+401_-55+402del	XP_011536201.1:n.-55+401_-55+402del
XR_245894.2:n.641-1183_641-1182del
XR_001748575.1:n.641-1183_641-1182del
NM_173353.4:c.541-1183_541-1182del MANE Select	NP_775489.2:n.541-1183_541-1182del