Canonical Allele Identifier: CA2089287634

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46845500_46845503delinsTTTG , CM000675.2:g.46845500_46845503delinsTTTG	GRCh38
NC_000013.10:g.47419635_47419638delinsTTTG , CM000675.1:g.47419635_47419638delinsTTTG	GRCh37
NC_000013.9:g.46317636_46317639delinsTTTG	NCBI36
NG_013011.1:g.56532_56535delinsCAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.614-9864_614-9861delinsCAAA MANE Select	ENSP00000437737.1:n.614-9864_614-9861delinsCAAA
ENST00000543956.5:c.125-9864_125-9861delinsCAAA	ENSP00000441861.2:n.125-9864_125-9861delinsCAAA
ENST00000378688.8:c.614-9864_614-9861delinsCAAA	ENSP00000367959.3:n.614-9864_614-9861delinsCAAA
ENST00000542664.3:c.614-9864_614-9861delinsCAAA	ENSP00000437737.1:n.614-9864_614-9861delinsCAAA
ENST00000543956.4:c.362-9864_362-9861delinsCAAA	ENSP00000441861.1:n.362-9864_362-9861delinsCAAA
NM_000621.4:c.614-9864_614-9861delinsCAAA	NP_000612.1:n.614-9864_614-9861delinsCAAA
NM_001165947.2:c.362-9864_362-9861delinsCAAA	NP_001159419.1:n.362-9864_362-9861delinsCAAA
NM_000621.5:c.614-9864_614-9861delinsCAAA MANE Select	NP_000612.1:n.614-9864_614-9861delinsCAAA
NM_001165947.5:c.125-9864_125-9861delinsCAAA	NP_001159419.2:n.125-9864_125-9861delinsCAAA
NM_001378924.1:c.614-9864_614-9861delinsCAAA	NP_001365853.1:n.614-9864_614-9861delinsCAAA