Canonical Allele Identifier: CA2001413506

Gene: HTR3A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113975355C= , CM000673.2:g.113975355C=	GRCh38
NC_000011.9:g.113846077C= , CM000673.1:g.113846077C=	GRCh37
NC_000011.8:g.113351287C=	NCBI36
NG_013058.1:g.5281C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504030.7:c.30C= MANE Select	ENSP00000424189.2:p.Leu10=
ENST00000355556.6:c.48C=	ENSP00000347754.2:p.Leu16=
ENST00000375498.6:c.48C=	ENSP00000364648.2:p.Leu16=
ENST00000504030.6:c.30C=	ENSP00000424189.2:p.Leu10=
ENST00000506841.6:c.30C=	ENSP00000424776.2:p.Leu10=
ENST00000510849.5:c.30C=	ENSP00000423653.1:p.Leu10=
NM_000869.5:c.48C=	NP_000860.2:p.Leu16=
NM_213621.3:c.48C=	NP_998786.2:p.Leu16=
NR_046363.1:n.281C=
NM_000869.6:c.30C= MANE Select	NP_000860.3:p.Leu10=
NM_213621.4:c.30C=	NP_998786.3:p.Leu10=
NR_046363.2:n.248C=