Canonical Allele Identifier: CA1955410087

Gene: TPH1

Linked Data

• dbSNP Id: rs1848014783

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18033585T>G , CM000673.2:g.18033585T>G	GRCh38
NC_000011.9:g.18055132T>G , CM000673.1:g.18055132T>G	GRCh37
NC_000011.8:g.18011708T>G	NCBI36
NG_011947.1:g.12204A>C
NG_011947.2:g.12204A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682019.1:c.302-211A>C MANE Select	ENSP00000508368.1:n.302-211A>C
ENST00000250018.6:c.302-211A>C	ENSP00000250018.2:n.302-211A>C
ENST00000417164.5:c.302-211A>C	ENSP00000403831.1:n.302-211A>C
ENST00000528338.1:c.332-211A>C	ENSP00000436081.1:n.332-211A>C
NM_004179.2:c.302-211A>C	NP_004170.1:n.302-211A>C
NM_004179.3:c.302-211A>C MANE Select	NP_004170.1:n.302-211A>C