Canonical Allele Identifier: CA1955410115
Gene: TPH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18033680_18033681delinsTC , CM000673.2:g.18033680_18033681delinsTC GRCh38
NC_000011.9:g.18055227_18055228delinsTC , CM000673.1:g.18055227_18055228delinsTC GRCh37
NC_000011.8:g.18011803_18011804delinsTC NCBI36
NG_011947.1:g.12108_12109delinsGA
NG_011947.2:g.12108_12109delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000682019.1:c.302-307_302-306delinsGA MANE Select ENSP00000508368.1:n.302-307_302-306delins...
ENST00000250018.6:c.302-307_302-306delinsGA ENSP00000250018.2:n.302-307_302-306delins...
ENST00000417164.5:c.302-307_302-306delinsGA ENSP00000403831.1:n.302-307_302-306delins...
ENST00000528338.1:c.332-307_332-306delinsGA ENSP00000436081.1:n.332-307_332-306delins...
NM_004179.2:c.302-307_302-306delinsGA NP_004170.1:n.302-307_302-306delinsGA
NM_004179.3:c.302-307_302-306delinsGA MANE Select NP_004170.1:n.302-307_302-306delinsGA