Canonical Allele Identifier: CA2799080101

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46834930_46834935del , CM000675.2:g.46834930_46834935del	GRCh38
NC_000013.10:g.47409065_47409070del , CM000675.1:g.47409065_47409070del	GRCh37
NC_000013.9:g.46307066_46307071del	NCBI36
NG_013011.1:g.67102_67107del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.1320_1325del MANE Select	ENSP00000437737.1:p.Asn441_Asp442del
ENST00000543956.5:c.831_836del	ENSP00000441861.2:p.Asn278_Asp279del
ENST00000378688.8:c.1320_1325del	ENSP00000367959.3:p.Asn441_Asp442del
ENST00000542664.3:c.1320_1325del	ENSP00000437737.1:p.Asn441_Asp442del
ENST00000543956.4:c.1068_1073del	ENSP00000441861.1:p.Asn357_Asp358del
NM_000621.4:c.1320_1325del	NP_000612.1:p.Asn441_Asp442del
NM_001165947.2:c.1068_1073del	NP_001159419.1:p.Asn357_Asp358del
NM_000621.5:c.1320_1325del MANE Select	NP_000612.1:p.Asn441_Asp442del
NM_001165947.5:c.831_836del	NP_001159419.2:p.Asn278_Asp279del
NM_001378924.1:c.1320_1325del	NP_001365853.1:p.Asn441_Asp442del