Canonical Allele Identifier: CA2045509798
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71941916_71941917delinsGC , CM000674.2:g.71941916_71941917delinsGC GRCh38
NC_000012.11:g.72335696_72335697delinsGC , CM000674.1:g.72335696_72335697delinsGC GRCh37
NC_000012.10:g.70621963_70621964delinsGC NCBI36
NG_008279.1:g.8071_8072delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.255+183_255+184delinsGC MANE Select ENSP00000329093.3:n.255+183_255+184delinsGC
ENST00000333850.3:c.255+183_255+184delinsGC ENSP00000329093.3:n.255+183_255+184delinsGC
ENST00000546576.1:n.265+183_265+184delinsGC
NM_173353.3:c.255+183_255+184delinsGC NP_775489.2:n.255+183_255+184delinsGC
XR_245894.2:n.355+183_355+184delinsGC
XR_001748575.1:n.355+183_355+184delinsGC
NM_173353.4:c.255+183_255+184delinsGC MANE Select NP_775489.2:n.255+183_255+184delinsGC