Canonical Allele Identifier: CA2045528206
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71983554_71983557delinsTCTC , CM000674.2:g.71983554_71983557delinsTCTC GRCh38
NC_000012.11:g.72377334_72377337delinsTCTC , CM000674.1:g.72377334_72377337delinsTCTC GRCh37
NC_000012.10:g.70663601_70663604delinsTCTC NCBI36
NG_008279.1:g.49709_49712delinsTCTC

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.941+4467_941+4470delinsTCTC MANE Select ENSP00000329093.3:n.941+4467_941+4470deli...
ENST00000333850.3:c.941+4467_941+4470delinsTCTC ENSP00000329093.3:n.941+4467_941+4470deli...
NM_173353.3:c.941+4467_941+4470delinsTCTC NP_775489.2:n.941+4467_941+4470delinsTCTC...
XM_011537899.1:c.347+4467_347+4470delinsTCTC XP_011536201.1:n.347+4467_347+4470delinsT...
NM_173353.4:c.941+4467_941+4470delinsTCTC MANE Select NP_775489.2:n.941+4467_941+4470delinsTCTC...