Canonical Allele Identifier: CA2045564922

Gene: TPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.72020892_72020893delinsTC , CM000674.2:g.72020892_72020893delinsTC	GRCh38
NC_000012.11:g.72414672_72414673delinsTC , CM000674.1:g.72414672_72414673delinsTC	GRCh37
NC_000012.10:g.70700939_70700940delinsTC	NCBI36
NG_008279.1:g.87047_87048delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333850.4:c.1069-1507_1069-1506delinsTC MANE Select	ENSP00000329093.3:n.1069-1507_1069-1506delinsTC
ENST00000333850.3:c.1069-1507_1069-1506delinsTC	ENSP00000329093.3:n.1069-1507_1069-1506delinsTC
NM_173353.3:c.1069-1507_1069-1506delinsTC	NP_775489.2:n.1069-1507_1069-1506delinsTC
XM_011537899.1:c.475-1507_475-1506delinsTC	XP_011536201.1:n.475-1507_475-1506delinsTC
NM_173353.4:c.1069-1507_1069-1506delinsTC MANE Select	NP_775489.2:n.1069-1507_1069-1506delinsTC