Canonical Allele Identifier: CA2045550691
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72010780_72010785delinsTTTTCA , CM000674.2:g.72010780_72010785delinsTTTTCA GRCh38
NC_000012.11:g.72404560_72404565delinsTTTTCA , CM000674.1:g.72404560_72404565delinsTTTTCA GRCh37
NC_000012.10:g.70690827_70690832delinsTTTTCA NCBI36
NG_008279.1:g.76935_76940delinsTTTTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1069-11619_1069-11614delinsTTTTCA MANE Select ENSP00000329093.3:n.1069-11619_1069-11614delinsTTTTCA
ENST00000333850.3:c.1069-11619_1069-11614delinsTTTTCA ENSP00000329093.3:n.1069-11619_1069-11614delinsTTTTCA
NM_173353.3:c.1069-11619_1069-11614delinsTTTTCA NP_775489.2:n.1069-11619_1069-11614delinsTTTTCA
XM_011537899.1:c.475-11619_475-11614delinsTTTTCA XP_011536201.1:n.475-11619_475-11614delinsTTTTCA
NM_173353.4:c.1069-11619_1069-11614delinsTTTTCA MANE Select NP_775489.2:n.1069-11619_1069-11614delinsTTTTCA