Canonical Allele Identifier: CA2089283681

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46835825_46835826delinsCT , CM000675.2:g.46835825_46835826delinsCT	GRCh38
NC_000013.10:g.47409960_47409961delinsCT , CM000675.1:g.47409960_47409961delinsCT	GRCh37
NC_000013.9:g.46307961_46307962delinsCT	NCBI36
NG_013011.1:g.66209_66210delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.614-187_614-186delinsAG MANE Select	ENSP00000437737.1:n.614-187_614-186delinsAG
ENST00000543956.5:c.125-187_125-186delinsAG	ENSP00000441861.2:n.125-187_125-186delinsAG
ENST00000378688.8:c.614-187_614-186delinsAG	ENSP00000367959.3:n.614-187_614-186delinsAG
ENST00000542664.3:c.614-187_614-186delinsAG	ENSP00000437737.1:n.614-187_614-186delinsAG
ENST00000543956.4:c.362-187_362-186delinsAG	ENSP00000441861.1:n.362-187_362-186delinsAG
NM_000621.4:c.614-187_614-186delinsAG	NP_000612.1:n.614-187_614-186delinsAG
NM_001165947.2:c.362-187_362-186delinsAG	NP_001159419.1:n.362-187_362-186delinsAG
NM_000621.5:c.614-187_614-186delinsAG MANE Select	NP_000612.1:n.614-187_614-186delinsAG
NM_001165947.5:c.125-187_125-186delinsAG	NP_001159419.2:n.125-187_125-186delinsAG
NM_001378924.1:c.614-187_614-186delinsAG	NP_001365853.1:n.614-187_614-186delinsAG