Canonical Allele Identifier: CA2045564872
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72020870_72020871delinsTG , CM000674.2:g.72020870_72020871delinsTG GRCh38
NC_000012.11:g.72414650_72414651delinsTG , CM000674.1:g.72414650_72414651delinsTG GRCh37
NC_000012.10:g.70700917_70700918delinsTG NCBI36
NG_008279.1:g.87025_87026delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1069-1529_1069-1528delinsTG MANE Select ENSP00000329093.3:n.1069-1529_1069-1528de...
ENST00000333850.3:c.1069-1529_1069-1528delinsTG ENSP00000329093.3:n.1069-1529_1069-1528de...
NM_173353.3:c.1069-1529_1069-1528delinsTG NP_775489.2:n.1069-1529_1069-1528delinsTG...
XM_011537899.1:c.475-1529_475-1528delinsTG XP_011536201.1:n.475-1529_475-1528delinsT...
NM_173353.4:c.1069-1529_1069-1528delinsTG MANE Select NP_775489.2:n.1069-1529_1069-1528delinsTG...