Canonical Allele Identifier: CA2796496212
Gene: TPH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994422_71994423insTTGGGTGTGTTTG , CM000674.2:g.71994422_71994423insTTGGGTGTGTTTG GRCh38
NC_000012.11:g.72388202_72388203insTTGGGTGTGTTTG , CM000674.1:g.72388202_72388203insTTGGGTGTGTTTG GRCh37
NC_000012.10:g.70674469_70674470insTTGGGTGTGTTTG NCBI36
NG_008279.1:g.60577_60578insTTGGGTGTGTTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.942-17_942-16insTTGGGTGTGTTTG MANE Select ENSP00000329093.3:n.942-17_942-16insTTGGGTGTGTTTG
ENST00000333850.3:c.942-17_942-16insTTGGGTGTGTTTG ENSP00000329093.3:n.942-17_942-16insTTGGGTGTGTTTG
NM_173353.3:c.942-17_942-16insTTGGGTGTGTTTG NP_775489.2:n.942-17_942-16insTTGGGTGTGTTTG
XM_011537899.1:c.348-17_348-16insTTGGGTGTGTTTG XP_011536201.1:n.348-17_348-16insTTGGGTGTGTTTG
NM_173353.4:c.942-17_942-16insTTGGGTGTGTTTG MANE Select NP_775489.2:n.942-17_942-16insTTGGGTGTGTTTG
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