Canonical Allele Identifier: CA2001397815

Gene: HTR3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932104_113932107delinsCTTA , CM000673.2:g.113932104_113932107delinsCTTA	GRCh38
NC_000011.9:g.113802826_113802829delinsCTTA , CM000673.1:g.113802826_113802829delinsCTTA	GRCh37
NC_000011.8:g.113308036_113308039delinsCTTA	NCBI36
NG_011483.1:g.32238_32241delinsCTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.369-185_369-182delinsCTTA MANE Select	ENSP00000260191.2:n.369-185_369-182delinsCTTA
ENST00000260191.7:c.369-185_369-182delinsCTTA	ENSP00000260191.2:n.369-185_369-182delinsCTTA
ENST00000260191.6:c.369-185_369-182delinsCTTA	ENSP00000260191.2:n.369-185_369-182delinsCTTA
ENST00000537778.5:c.336-185_336-182delinsCTTA	ENSP00000443118.1:n.336-185_336-182delinsCTTA
ENST00000543092.1:c.155-185_155-182delinsCTTA
NM_006028.4:c.369-185_369-182delinsCTTA	NP_006019.1:n.369-185_369-182delinsCTTA
XM_011543063.1:c.336-185_336-182delinsCTTA	XP_011541365.1:n.336-185_336-182delinsCTTA
XM_011543064.1:c.168-185_168-182delinsCTTA	XP_011541366.1:n.168-185_168-182delinsCTTA
XM_011543065.1:c.162-185_162-182delinsCTTA	XP_011541367.1:n.162-185_162-182delinsCTTA
XM_011543066.1:c.336-185_336-182delinsCTTA	XP_011541368.1:n.336-185_336-182delinsCTTA
NM_001363563.1:c.336-185_336-182delinsCTTA	NP_001350492.1:n.336-185_336-182delinsCTTA
XM_017018552.2:c.162-185_162-182delinsCTTA	XP_016874041.1:n.162-185_162-182delinsCTTA
XM_024448767.1:c.75-185_75-182delinsCTTA	XP_024304535.1:n.75-185_75-182delinsCTTA
XR_001748034.2:n.620-185_620-182delinsCTTA
NM_001363563.2:c.336-185_336-182delinsCTTA	NP_001350492.1:n.336-185_336-182delinsCTTA
NM_006028.5:c.369-185_369-182delinsCTTA MANE Select	NP_006019.1:n.369-185_369-182delinsCTTA