Canonical Allele Identifier: CA388150578

Gene: HTR2A

Linked Data

• gnomAD v4: 13-46834976-A-T
• MyVariant Identifiers: chr13:g.47409111A>T (hg19) ; chr13:g.46834976A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46834976A>T , CM000675.2:g.46834976A>T	GRCh38
NC_000013.10:g.47409111A>T , CM000675.1:g.47409111A>T	GRCh37
NC_000013.9:g.46307112A>T	NCBI36
NG_013011.1:g.67059T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.1277T>A MANE Select	ENSP00000437737.1:p.Met426Lys
ENST00000543956.5:c.788T>A	ENSP00000441861.2:p.Met263Lys
ENST00000378688.8:c.1277T>A	ENSP00000367959.3:p.Met426Lys
ENST00000542664.3:c.1277T>A	ENSP00000437737.1:p.Met426Lys
ENST00000543956.4:c.1025T>A	ENSP00000441861.1:p.Met342Lys
NM_000621.4:c.1277T>A	NP_000612.1:p.Met426Lys
NM_001165947.2:c.1025T>A	NP_001159419.1:p.Met342Lys
NM_000621.5:c.1277T>A MANE Select	NP_000612.1:p.Met426Lys
NM_001165947.5:c.788T>A	NP_001159419.2:p.Met263Lys
NM_001378924.1:c.1277T>A	NP_001365853.1:p.Met426Lys