Canonical Allele Identifier: CA2045564781
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72020825_72020826delinsGA , CM000674.2:g.72020825_72020826delinsGA GRCh38
NC_000012.11:g.72414605_72414606delinsGA , CM000674.1:g.72414605_72414606delinsGA GRCh37
NC_000012.10:g.70700872_70700873delinsGA NCBI36
NG_008279.1:g.86980_86981delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1069-1574_1069-1573delinsGA MANE Select ENSP00000329093.3:n.1069-1574_1069-1573delinsGA
ENST00000333850.3:c.1069-1574_1069-1573delinsGA ENSP00000329093.3:n.1069-1574_1069-1573delinsGA
NM_173353.3:c.1069-1574_1069-1573delinsGA NP_775489.2:n.1069-1574_1069-1573delinsGA
XM_011537899.1:c.475-1574_475-1573delinsGA XP_011536201.1:n.475-1574_475-1573delinsGA
NM_173353.4:c.1069-1574_1069-1573delinsGA MANE Select NP_775489.2:n.1069-1574_1069-1573delinsGA