Canonical Allele Identifier: CA1955404384
Gene: TPH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18019087T= , CM000673.2:g.18019087T= GRCh38
NC_000011.9:g.18040634T= , CM000673.1:g.18040634T= GRCh37
NC_000011.8:g.17997210T= NCBI36
NG_011947.1:g.26702A=
NG_011947.2:g.26702A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682019.1:c.*1904A= MANE Select ENSP00000508368.1:n.*1904A=
ENST00000250018.6:c.*1904A= ENSP00000250018.2:n.*1904A=
NM_004179.3:c.*1904A= MANE Select NP_004170.1:n.*1904A=