Canonical Allele Identifier: CA1955410111
Gene: TPH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18033671_18033675delinsTTTAG , CM000673.2:g.18033671_18033675delinsTTTAG GRCh38
NC_000011.9:g.18055218_18055222delinsTTTAG , CM000673.1:g.18055218_18055222delinsTTTAG GRCh37
NC_000011.8:g.18011794_18011798delinsTTTAG NCBI36
NG_011947.1:g.12114_12118delinsCTAAA
NG_011947.2:g.12114_12118delinsCTAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000682019.1:c.302-301_302-297delinsCTAAA MANE Select ENSP00000508368.1:n.302-301_302-297delins...
ENST00000250018.6:c.302-301_302-297delinsCTAAA ENSP00000250018.2:n.302-301_302-297delins...
ENST00000417164.5:c.302-301_302-297delinsCTAAA ENSP00000403831.1:n.302-301_302-297delins...
ENST00000528338.1:c.332-301_332-297delinsCTAAA ENSP00000436081.1:n.332-301_332-297delins...
NM_004179.2:c.302-301_302-297delinsCTAAA NP_004170.1:n.302-301_302-297delinsCTAAA
NM_004179.3:c.302-301_302-297delinsCTAAA MANE Select NP_004170.1:n.302-301_302-297delinsCTAAA