Canonical Allele Identifier: CA2796495958

Gene: TPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71983361del , CM000674.2:g.71983361del	GRCh38
NC_000012.11:g.72377141del , CM000674.1:g.72377141del	GRCh37
NC_000012.10:g.70663408del	NCBI36
NG_008279.1:g.49516del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333850.4:c.941+4274del MANE Select	ENSP00000329093.3:n.941+4274del
ENST00000333850.3:c.941+4274del	ENSP00000329093.3:n.941+4274del
NM_173353.3:c.941+4274del	NP_775489.2:n.941+4274del
XM_011537899.1:c.347+4274del	XP_011536201.1:n.347+4274del
NM_173353.4:c.941+4274del MANE Select	NP_775489.2:n.941+4274del