Canonical Allele Identifier: CA1955410098
Gene: TPH1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18033613G= , CM000673.2:g.18033613G= GRCh38
NC_000011.9:g.18055160G= , CM000673.1:g.18055160G= GRCh37
NC_000011.8:g.18011736G= NCBI36
NG_011947.1:g.12176C=
NG_011947.2:g.12176C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682019.1:c.302-239C= MANE Select ENSP00000508368.1:n.302-239C=
ENST00000250018.6:c.302-239C= ENSP00000250018.2:n.302-239C=
ENST00000417164.5:c.302-239C= ENSP00000403831.1:n.302-239C=
ENST00000528338.1:c.332-239C= ENSP00000436081.1:n.332-239C=
NM_004179.2:c.302-239C= NP_004170.1:n.302-239C=
NM_004179.3:c.302-239C= MANE Select NP_004170.1:n.302-239C=
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