Canonical Allele Identifier: CA2508039104
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72020604_72020605del , CM000674.2:g.72020604_72020605del GRCh38
NC_000012.11:g.72414384_72414385del , CM000674.1:g.72414384_72414385del GRCh37
NC_000012.10:g.70700651_70700652del NCBI36
NG_008279.1:g.86759_86760del

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1069-1795_1069-1794del MANE Select ENSP00000329093.3:n.1069-1795_1069-1794de...
ENST00000333850.3:c.1069-1795_1069-1794del ENSP00000329093.3:n.1069-1795_1069-1794de...
NM_173353.3:c.1069-1795_1069-1794del NP_775489.2:n.1069-1795_1069-1794del
XM_011537899.1:c.475-1795_475-1794del XP_011536201.1:n.475-1795_475-1794del
NM_173353.4:c.1069-1795_1069-1794del MANE Select NP_775489.2:n.1069-1795_1069-1794del