Canonical Allele Identifier: CA218516614
Gene: TPH1 HGNC NCBI

Linked Data

dbSNP Id: rs965331883

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18033788del , CM000673.2:g.18033788del GRCh38
NC_000011.9:g.18055335del , CM000673.1:g.18055335del GRCh37
NC_000011.8:g.18011911del NCBI36
NG_011947.1:g.12001del
NG_011947.2:g.12001del

Transcript Alleles

HGVS Amino-acid change
ENST00000682019.1:c.302-414del MANE Select ENSP00000508368.1:n.302-414del
ENST00000250018.6:c.302-414del ENSP00000250018.2:n.302-414del
ENST00000417164.5:c.302-414del ENSP00000403831.1:n.302-414del
ENST00000528338.1:c.332-414del ENSP00000436081.1:n.332-414del
NM_004179.2:c.302-414del NP_004170.1:n.302-414del
NM_004179.3:c.302-414del MANE Select NP_004170.1:n.302-414del