Canonical Allele Identifier: CA1955404393
Gene: TPH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18019113A= , CM000673.2:g.18019113A= GRCh38
NC_000011.9:g.18040660A= , CM000673.1:g.18040660A= GRCh37
NC_000011.8:g.17997236A= NCBI36
NG_011947.1:g.26676T=
NG_011947.2:g.26676T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682019.1:c.*1878T= MANE Select ENSP00000508368.1:n.*1878T=
ENST00000250018.6:c.*1878T= ENSP00000250018.2:n.*1878T=
NM_004179.3:c.*1878T= MANE Select NP_004170.1:n.*1878T=