Canonical Allele Identifier: CA2045551152
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.72011115_72011122delinsGGTAGCTA , CM000674.2:g.72011115_72011122delinsGGTAGCTA GRCh38
NC_000012.11:g.72404895_72404902delinsGGTAGCTA , CM000674.1:g.72404895_72404902delinsGGTAGCTA GRCh37
NC_000012.10:g.70691162_70691169delinsGGTAGCTA NCBI36
NG_008279.1:g.77270_77277delinsGGTAGCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.1069-11284_1069-11277delinsGGTAGCTA MANE Select ENSP00000329093.3:n.1069-11284_1069-11277delinsGGTAGCTA
ENST00000333850.3:c.1069-11284_1069-11277delinsGGTAGCTA ENSP00000329093.3:n.1069-11284_1069-11277delinsGGTAGCTA
NM_173353.3:c.1069-11284_1069-11277delinsGGTAGCTA NP_775489.2:n.1069-11284_1069-11277delinsGGTAGCTA
XM_011537899.1:c.475-11284_475-11277delinsGGTAGCTA XP_011536201.1:n.475-11284_475-11277delinsGGTAGCTA
NM_173353.4:c.1069-11284_1069-11277delinsGGTAGCTA MANE Select NP_775489.2:n.1069-11284_1069-11277delinsGGTAGCTA