Canonical Allele Identifier: CA1955404394
Gene: TPH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18019114C= , CM000673.2:g.18019114C= GRCh38
NC_000011.9:g.18040661C= , CM000673.1:g.18040661C= GRCh37
NC_000011.8:g.17997237C= NCBI36
NG_011947.1:g.26675G=
NG_011947.2:g.26675G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682019.1:c.*1877G= MANE Select ENSP00000508368.1:n.*1877G=
ENST00000250018.6:c.*1877G= ENSP00000250018.2:n.*1877G=
NM_004179.3:c.*1877G= MANE Select NP_004170.1:n.*1877G=