Canonical Allele Identifier: CA2045510749
Gene: TPH2 HGNC NCBI

Linked Data

dbSNP Id: rs1871109872

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71942847del , CM000674.2:g.71942847del GRCh38
NC_000012.11:g.72336627del , CM000674.1:g.72336627del GRCh37
NC_000012.10:g.70622894del NCBI36
NG_008279.1:g.9002del

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.255+1114del MANE Select ENSP00000329093.3:n.255+1114del
ENST00000333850.3:c.255+1114del ENSP00000329093.3:n.255+1114del
ENST00000546576.1:n.265+1114del
NM_173353.3:c.255+1114del NP_775489.2:n.255+1114del
XR_245894.2:n.355+1114del
XR_001748575.1:n.355+1114del
NM_173353.4:c.255+1114del MANE Select NP_775489.2:n.255+1114del