Canonical Allele Identifier: CA2045562042
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72018765_72018781delinsCTAGTTTTCCTCCATTT , CM000674.2:g.72018765_72018781delinsCTAGTTTTCCTCCATTT GRCh38
NC_000012.11:g.72412545_72412561delinsCTAGTTTTCCTCCATTT , CM000674.1:g.72412545_72412561delinsCTAGTTTTCCTCCATTT GRCh37
NC_000012.10:g.70698812_70698828delinsCTAGTTTTCCTCCATTT NCBI36
NG_008279.1:g.84920_84936delinsCTAGTTTTCCTCCATTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1069-3634_1069-3618delinsCTAGTTTTCCTCCATTT MANE Select ENSP00000329093.3:n.1069-3634_1069-3618delinsCTAGTTTTCCTCCATT...
ENST00000333850.3:c.1069-3634_1069-3618delinsCTAGTTTTCCTCCATTT ENSP00000329093.3:n.1069-3634_1069-3618delinsCTAGTTTTCCTCCATT...
NM_173353.3:c.1069-3634_1069-3618delinsCTAGTTTTCCTCCATTT NP_775489.2:n.1069-3634_1069-3618delinsCTAGTTTTCCTCCATTT
XM_011537899.1:c.475-3634_475-3618delinsCTAGTTTTCCTCCATTT XP_011536201.1:n.475-3634_475-3618delinsCTAGTTTTCCTCCATTT
NM_173353.4:c.1069-3634_1069-3618delinsCTAGTTTTCCTCCATTT MANE Select NP_775489.2:n.1069-3634_1069-3618delinsCTAGTTTTCCTCCATTT