Canonical Allele Identifier: CA2045510956
Gene: TPH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71943054_71943055delinsCA , CM000674.2:g.71943054_71943055delinsCA GRCh38
NC_000012.11:g.72336834_72336835delinsCA , CM000674.1:g.72336834_72336835delinsCA GRCh37
NC_000012.10:g.70623101_70623102delinsCA NCBI36
NG_008279.1:g.9209_9210delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000333850.4:c.256-1240_256-1239delinsCA MANE Select ENSP00000329093.3:n.256-1240_256-1239delinsCA
ENST00000333850.3:c.256-1240_256-1239delinsCA ENSP00000329093.3:n.256-1240_256-1239delinsCA
ENST00000546576.1:n.266-1240_266-1239delinsCA
NM_173353.3:c.256-1240_256-1239delinsCA NP_775489.2:n.256-1240_256-1239delinsCA
XR_245894.2:n.356-1240_356-1239delinsCA
XR_001748575.1:n.356-1240_356-1239delinsCA
NM_173353.4:c.256-1240_256-1239delinsCA MANE Select NP_775489.2:n.256-1240_256-1239delinsCA