Canonical Allele Identifier: CA2045533090

Gene: TPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71994518C= , CM000674.2:g.71994518C=	GRCh38
NC_000012.11:g.72388298C= , CM000674.1:g.72388298C=	GRCh37
NC_000012.10:g.70674565C=	NCBI36
NG_008279.1:g.60673C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333850.4:c.1021C= MANE Select	ENSP00000329093.3:p.Leu341=
ENST00000333850.3:c.1021C=	ENSP00000329093.3:p.Leu341=
NM_173353.3:c.1021C=	NP_775489.2:p.Leu341=
XM_011537899.1:c.427C=	XP_011536201.1:p.Leu143=
NM_173353.4:c.1021C= MANE Select	NP_775489.2:p.Leu341=