Canonical Allele Identifier: CA2045550341
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72010507_72010510delinsTAAA , CM000674.2:g.72010507_72010510delinsTAAA GRCh38
NC_000012.11:g.72404287_72404290delinsTAAA , CM000674.1:g.72404287_72404290delinsTAAA GRCh37
NC_000012.10:g.70690554_70690557delinsTAAA NCBI36
NG_008279.1:g.76662_76665delinsTAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1069-11892_1069-11889delinsTAAA MANE Select ENSP00000329093.3:n.1069-11892_1069-11889delinsTAAA
ENST00000333850.3:c.1069-11892_1069-11889delinsTAAA ENSP00000329093.3:n.1069-11892_1069-11889delinsTAAA
NM_173353.3:c.1069-11892_1069-11889delinsTAAA NP_775489.2:n.1069-11892_1069-11889delinsTAAA
XM_011537899.1:c.475-11892_475-11889delinsTAAA XP_011536201.1:n.475-11892_475-11889delinsTAAA
NM_173353.4:c.1069-11892_1069-11889delinsTAAA MANE Select NP_775489.2:n.1069-11892_1069-11889delinsTAAA