Canonical Allele Identifier: CA2045510975
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71943068_71943069delinsAG , CM000674.2:g.71943068_71943069delinsAG GRCh38
NC_000012.11:g.72336848_72336849delinsAG , CM000674.1:g.72336848_72336849delinsAG GRCh37
NC_000012.10:g.70623115_70623116delinsAG NCBI36
NG_008279.1:g.9223_9224delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.256-1226_256-1225delinsAG MANE Select ENSP00000329093.3:n.256-1226_256-1225delinsAG
ENST00000333850.3:c.256-1226_256-1225delinsAG ENSP00000329093.3:n.256-1226_256-1225delinsAG
ENST00000546576.1:n.266-1226_266-1225delinsAG
NM_173353.3:c.256-1226_256-1225delinsAG NP_775489.2:n.256-1226_256-1225delinsAG
XR_245894.2:n.356-1226_356-1225delinsAG
XR_001748575.1:n.356-1226_356-1225delinsAG
NM_173353.4:c.256-1226_256-1225delinsAG MANE Select NP_775489.2:n.256-1226_256-1225delinsAG