Canonical Allele Identifier: CA1955404342
Gene: TPH1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18018953T= , CM000673.2:g.18018953T= GRCh38
NC_000011.9:g.18040500T= , CM000673.1:g.18040500T= GRCh37
NC_000011.8:g.17997076T= NCBI36
NG_011947.1:g.26836A=
NG_011947.2:g.26836A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682019.1:c.*2038A= MANE Select ENSP00000508368.1:n.*2038A=
ENST00000250018.6:c.*2038A= ENSP00000250018.2:n.*2038A=
NM_004179.3:c.*2038A= MANE Select NP_004170.1:n.*2038A=
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