Canonical Allele Identifier: CA2045561833

Gene: TPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.72018622_72018623delinsGC , CM000674.2:g.72018622_72018623delinsGC	GRCh38
NC_000012.11:g.72412402_72412403delinsGC , CM000674.1:g.72412402_72412403delinsGC	GRCh37
NC_000012.10:g.70698669_70698670delinsGC	NCBI36
NG_008279.1:g.84777_84778delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333850.4:c.1069-3777_1069-3776delinsGC MANE Select	ENSP00000329093.3:n.1069-3777_1069-3776delinsGC
ENST00000333850.3:c.1069-3777_1069-3776delinsGC	ENSP00000329093.3:n.1069-3777_1069-3776delinsGC
NM_173353.3:c.1069-3777_1069-3776delinsGC	NP_775489.2:n.1069-3777_1069-3776delinsGC
XM_011537899.1:c.475-3777_475-3776delinsGC	XP_011536201.1:n.475-3777_475-3776delinsGC
NM_173353.4:c.1069-3777_1069-3776delinsGC MANE Select	NP_775489.2:n.1069-3777_1069-3776delinsGC