Canonical Allele Identifier: CA218516555
Gene: TPH1 HGNC NCBI

Linked Data

dbSNP Id: rs906170778

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18033585dup , CM000673.2:g.18033585dup GRCh38
NC_000011.9:g.18055132dup , CM000673.1:g.18055132dup GRCh37
NC_000011.8:g.18011708dup NCBI36
NG_011947.1:g.12212dup
NG_011947.2:g.12212dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000682019.1:c.302-203dup MANE Select ENSP00000508368.1:n.302-203dup
ENST00000250018.6:c.302-203dup ENSP00000250018.2:n.302-203dup
ENST00000417164.5:c.302-203dup ENSP00000403831.1:n.302-203dup
ENST00000528338.1:c.332-203dup ENSP00000436081.1:n.332-203dup
NM_004179.2:c.302-203dup NP_004170.1:n.302-203dup
NM_004179.3:c.302-203dup MANE Select NP_004170.1:n.302-203dup