Canonical Allele Identifier: CA2045528121

Gene: TPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71983385_71983386delinsTA , CM000674.2:g.71983385_71983386delinsTA	GRCh38
NC_000012.11:g.72377165_72377166delinsTA , CM000674.1:g.72377165_72377166delinsTA	GRCh37
NC_000012.10:g.70663432_70663433delinsTA	NCBI36
NG_008279.1:g.49540_49541delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333850.4:c.941+4298_941+4299delinsTA MANE Select	ENSP00000329093.3:n.941+4298_941+4299delinsTA
ENST00000333850.3:c.941+4298_941+4299delinsTA	ENSP00000329093.3:n.941+4298_941+4299delinsTA
NM_173353.3:c.941+4298_941+4299delinsTA	NP_775489.2:n.941+4298_941+4299delinsTA
XM_011537899.1:c.347+4298_347+4299delinsTA	XP_011536201.1:n.347+4298_347+4299delinsTA
NM_173353.4:c.941+4298_941+4299delinsTA MANE Select	NP_775489.2:n.941+4298_941+4299delinsTA