Canonical Allele Identifier: CA2045533129
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994620_71994621delinsAG , CM000674.2:g.71994620_71994621delinsAG GRCh38
NC_000012.11:g.72388400_72388401delinsAG , CM000674.1:g.72388400_72388401delinsAG GRCh37
NC_000012.10:g.70674667_70674668delinsAG NCBI36
NG_008279.1:g.60775_60776delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1068+55_1068+56delinsAG MANE Select ENSP00000329093.3:n.1068+55_1068+56delins...
ENST00000333850.3:c.1068+55_1068+56delinsAG ENSP00000329093.3:n.1068+55_1068+56delins...
NM_173353.3:c.1068+55_1068+56delinsAG NP_775489.2:n.1068+55_1068+56delinsAG
XM_011537899.1:c.474+55_474+56delinsAG XP_011536201.1:n.474+55_474+56delinsAG
NM_173353.4:c.1068+55_1068+56delinsAG MANE Select NP_775489.2:n.1068+55_1068+56delinsAG