Canonical Allele Identifier: CA477044783

Gene: HTR3A

Genomic Alleles

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

Transcript Alleles

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