Canonical Allele Identifier: CA2001397983

Gene: HTR3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932439_113932440delinsCA , CM000673.2:g.113932439_113932440delinsCA	GRCh38
NC_000011.9:g.113803161_113803162delinsCA , CM000673.1:g.113803161_113803162delinsCA	GRCh37
NC_000011.8:g.113308371_113308372delinsCA	NCBI36
NG_011483.1:g.32573_32574delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.519_520delinsCA MANE Select	ENSP00000260191.2:p.Phe173=
ENST00000260191.7:c.519_520delinsCA	ENSP00000260191.2:p.Phe173=
ENST00000260191.6:c.519_520delinsCA	ENSP00000260191.2:p.Phe173=
ENST00000537778.5:c.486_487delinsCA	ENSP00000443118.1:p.Phe162=
ENST00000543092.1:c.305_306delinsCA
NM_006028.4:c.519_520delinsCA	NP_006019.1:p.Phe173=
XM_011543063.1:c.486_487delinsCA	XP_011541365.1:p.Phe162=
XM_011543064.1:c.318_319delinsCA	XP_011541366.1:p.Phe106=
XM_011543065.1:c.312_313delinsCA	XP_011541367.1:p.Phe104=
XM_011543066.1:c.486_487delinsCA	XP_011541368.1:p.Phe162=
NM_001363563.1:c.486_487delinsCA	NP_001350492.1:p.Phe162=
XM_017018552.2:c.312_313delinsCA	XP_016874041.1:p.Phe104=
XM_024448767.1:c.225_226delinsCA	XP_024304535.1:p.Phe75=
XR_001748034.2:n.770_771delinsCA
NM_001363563.2:c.486_487delinsCA	NP_001350492.1:p.Phe162=
NM_006028.5:c.519_520delinsCA MANE Select	NP_006019.1:p.Phe173=