Canonical Allele Identifier: CA388148441

Gene: HTR2A

Linked Data

• dbSNP Id: rs539412303
• MyVariant Identifiers: chr13:g.47435426_47435427insCC (hg19) ; chr13:g.46861291_46861292insCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46861292_46861293insCC , CM000675.2:g.46861292_46861293insCC	GRCh38
NC_000013.10:g.47435427_47435428insCC , CM000675.1:g.47435427_47435428insCC	GRCh37
NC_000013.9:g.46333428_46333429insCC	NCBI36
NG_013011.1:g.40743_40744insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.614-25653_614-25652insGG MANE Select	ENSP00000437737.1:n.614-25653_614-25652insGG
ENST00000543956.5:c.125-25653_125-25652insGG	ENSP00000441861.2:n.125-25653_125-25652insGG
ENST00000378688.8:c.614-25653_614-25652insGG	ENSP00000367959.3:n.614-25653_614-25652insGG
ENST00000542664.3:c.614-25653_614-25652insGG	ENSP00000437737.1:n.614-25653_614-25652insGG
ENST00000543956.4:c.362-25653_362-25652insGG	ENSP00000441861.1:n.362-25653_362-25652insGG
NM_000621.4:c.614-25653_614-25652insGG	NP_000612.1:n.614-25653_614-25652insGG
NM_001165947.2:c.362-25653_362-25652insGG	NP_001159419.1:n.362-25653_362-25652insGG
NM_000621.5:c.614-25653_614-25652insGG MANE Select	NP_000612.1:n.614-25653_614-25652insGG
NM_001165947.5:c.125-25653_125-25652insGG	NP_001159419.2:n.125-25653_125-25652insGG
NM_001378924.1:c.614-25653_614-25652insGG	NP_001365853.1:n.614-25653_614-25652insGG