Canonical Allele Identifier: CA2045509823
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71941939_71941941delinsCAG , CM000674.2:g.71941939_71941941delinsCAG GRCh38
NC_000012.11:g.72335719_72335721delinsCAG , CM000674.1:g.72335719_72335721delinsCAG GRCh37
NC_000012.10:g.70621986_70621988delinsCAG NCBI36
NG_008279.1:g.8094_8096delinsCAG

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.255+206_255+208delinsCAG MANE Select ENSP00000329093.3:n.255+206_255+208delinsCAG
ENST00000333850.3:c.255+206_255+208delinsCAG ENSP00000329093.3:n.255+206_255+208delinsCAG
ENST00000546576.1:n.265+206_265+208delinsCAG
NM_173353.3:c.255+206_255+208delinsCAG NP_775489.2:n.255+206_255+208delinsCAG
XR_245894.2:n.355+206_355+208delinsCAG
XR_001748575.1:n.355+206_355+208delinsCAG
NM_173353.4:c.255+206_255+208delinsCAG MANE Select NP_775489.2:n.255+206_255+208delinsCAG