Canonical Allele Identifier: CA2001417294

Gene: HTR3A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113989703A= , CM000673.2:g.113989703A=	GRCh38
NC_000011.9:g.113860425A= , CM000673.1:g.113860425A=	GRCh37
NC_000011.8:g.113365635A=	NCBI36
NG_013058.1:g.19629A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000869.6:c.1377A= MANE Select	NP_000860.3:p.Leu459=
ENST00000504030.7:c.1377A= MANE Select	ENSP00000424189.2:p.Leu459=
NM_000869.5:c.1395A=	NP_000860.2:p.Leu465=
NM_001161772.2:c.1332A=	NP_001155244.1:p.Leu444=
NM_001161772.3:c.1332A=	NP_001155244.1:p.Leu444=
NM_213621.3:c.1491A=	NP_998786.2:p.Leu497=
NM_213621.4:c.1473A=	NP_998786.3:p.Leu491=
NR_046363.1:n.1467A=
NR_046363.2:n.1434A=
ENST00000299961.5:c.1332A=	ENSP00000299961.4:p.Leu444=
ENST00000355556.6:c.1491A=	ENSP00000347754.2:p.Leu497=
ENST00000375498.6:c.1395A=	ENSP00000364648.2:p.Leu465=
ENST00000504030.6:c.1377A=	ENSP00000424189.2:p.Leu459=
ENST00000506841.6:c.1473A=	ENSP00000424776.2:p.Leu491=
ENST00000510849.5:c.*499A=	ENSP00000423653.1:n.*499A=