Canonical Allele Identifier: CA2001397800

Gene: HTR3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932067_113932070delinsCATT , CM000673.2:g.113932067_113932070delinsCATT	GRCh38
NC_000011.9:g.113802789_113802792delinsCATT , CM000673.1:g.113802789_113802792delinsCATT	GRCh37
NC_000011.8:g.113307999_113308002delinsCATT	NCBI36
NG_011483.1:g.32201_32204delinsCATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.368+200_368+203delinsCATT MANE Select	ENSP00000260191.2:n.368+200_368+203delinsCATT
ENST00000260191.7:c.368+200_368+203delinsCATT	ENSP00000260191.2:n.368+200_368+203delinsCATT
ENST00000260191.6:c.368+200_368+203delinsCATT	ENSP00000260191.2:n.368+200_368+203delinsCATT
ENST00000537778.5:c.335+200_335+203delinsCATT	ENSP00000443118.1:n.335+200_335+203delinsCATT
ENST00000543092.1:c.154+200_154+203delinsCATT
NM_006028.4:c.368+200_368+203delinsCATT	NP_006019.1:n.368+200_368+203delinsCATT
XM_011543063.1:c.335+200_335+203delinsCATT	XP_011541365.1:n.335+200_335+203delinsCATT
XM_011543064.1:c.167+200_167+203delinsCATT	XP_011541366.1:n.167+200_167+203delinsCATT
XM_011543065.1:c.161+200_161+203delinsCATT	XP_011541367.1:n.161+200_161+203delinsCATT
XM_011543066.1:c.335+200_335+203delinsCATT	XP_011541368.1:n.335+200_335+203delinsCATT
NM_001363563.1:c.335+200_335+203delinsCATT	NP_001350492.1:n.335+200_335+203delinsCATT
XM_017018552.2:c.161+200_161+203delinsCATT	XP_016874041.1:n.161+200_161+203delinsCATT
XM_024448767.1:c.74+200_74+203delinsCATT	XP_024304535.1:n.74+200_74+203delinsCATT
XR_001748034.2:n.619+200_619+203delinsCATT
NM_001363563.2:c.335+200_335+203delinsCATT	NP_001350492.1:n.335+200_335+203delinsCATT
NM_006028.5:c.368+200_368+203delinsCATT MANE Select	NP_006019.1:n.368+200_368+203delinsCATT