Canonical Allele Identifier: CA218519028
Gene: TPH1 HGNC NCBI

Linked Data

dbSNP Id: rs370463901

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18018951del , CM000673.2:g.18018951del GRCh38
NC_000011.9:g.18040498del , CM000673.1:g.18040498del GRCh37
NC_000011.8:g.17997074del NCBI36
NG_011947.1:g.26844del
NG_011947.2:g.26844del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682019.1:c.*2046del MANE Select ENSP00000508368.1:n.*2046del
ENST00000250018.6:c.*2046del ENSP00000250018.2:n.*2046del
NM_004179.3:c.*2046del MANE Select NP_004170.1:n.*2046del