Canonical Allele Identifier: CA1955404382
Gene: TPH1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18019084A= , CM000673.2:g.18019084A= GRCh38
NC_000011.9:g.18040631A= , CM000673.1:g.18040631A= GRCh37
NC_000011.8:g.17997207A= NCBI36
NG_011947.1:g.26705T=
NG_011947.2:g.26705T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682019.1:c.*1907T= MANE Select ENSP00000508368.1:n.*1907T=
ENST00000250018.6:c.*1907T= ENSP00000250018.2:n.*1907T=
NM_004179.3:c.*1907T= MANE Select NP_004170.1:n.*1907T=
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