Canonical Allele Identifier: CA6284376

Gene: HTR3A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113977551A>T , CM000673.2:g.113977551A>T	GRCh38
NC_000011.9:g.113848273A>T , CM000673.1:g.113848273A>T	GRCh37
NC_000011.8:g.113353483A>T	NCBI36
NG_013058.1:g.7477A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000869.6:c.68-220A>T MANE Select	NP_000860.3:n.68-220A>T
ENST00000504030.7:c.68-220A>T MANE Select	ENSP00000424189.2:n.68-220A>T
NM_000869.5:c.86-220A>T	NP_000860.2:n.86-220A>T
NM_001161772.2:c.-4A>T	NP_001155244.1:n.-4A>T
NM_001161772.3:c.-4A>T	NP_001155244.1:n.-4A>T
NM_213621.3:c.86-220A>T	NP_998786.2:n.86-220A>T
NM_213621.4:c.68-220A>T	NP_998786.3:n.68-220A>T
NR_046363.1:n.319-220A>T
NR_046363.2:n.286-220A>T
ENST00000299961.5:c.-4A>T	ENSP00000299961.4:n.-4A>T
ENST00000355556.6:c.86-220A>T	ENSP00000347754.2:n.86-220A>T
ENST00000375498.6:c.86-220A>T	ENSP00000364648.2:n.86-220A>T
ENST00000504030.6:c.68-220A>T	ENSP00000424189.2:n.68-220A>T
ENST00000506841.6:c.68-220A>T	ENSP00000424776.2:n.68-220A>T
ENST00000510849.5:c.68-220A>T	ENSP00000423653.1:n.68-220A>T