Canonical Allele Identifier: CA1955410129
Gene: TPH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18033722C= , CM000673.2:g.18033722C= GRCh38
NC_000011.9:g.18055269C= , CM000673.1:g.18055269C= GRCh37
NC_000011.8:g.18011845C= NCBI36
NG_011947.1:g.12067G=
NG_011947.2:g.12067G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682019.1:c.302-348G= MANE Select ENSP00000508368.1:n.302-348G=
ENST00000250018.6:c.302-348G= ENSP00000250018.2:n.302-348G=
ENST00000417164.5:c.302-348G= ENSP00000403831.1:n.302-348G=
ENST00000528338.1:c.332-348G= ENSP00000436081.1:n.332-348G=
NM_004179.2:c.302-348G= NP_004170.1:n.302-348G=
NM_004179.3:c.302-348G= MANE Select NP_004170.1:n.302-348G=