Canonical Allele Identifier: CA2089283718

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46835915_46835920delinsAATATT , CM000675.2:g.46835915_46835920delinsAATATT	GRCh38
NC_000013.10:g.47410050_47410055delinsAATATT , CM000675.1:g.47410050_47410055delinsAATATT	GRCh37
NC_000013.9:g.46308051_46308056delinsAATATT	NCBI36
NG_013011.1:g.66115_66120delinsAATATT

Transcript Alleles

HGVS	Amino-acid change
ENST00000542664.4:c.614-281_614-276delinsAATATT MANE Select	ENSP00000437737.1:n.614-281_614-276delins...
ENST00000543956.5:c.125-281_125-276delinsAATATT	ENSP00000441861.2:n.125-281_125-276delins...
ENST00000378688.8:c.614-281_614-276delinsAATATT	ENSP00000367959.3:n.614-281_614-276delins...
ENST00000542664.3:c.614-281_614-276delinsAATATT	ENSP00000437737.1:n.614-281_614-276delins...
ENST00000543956.4:c.362-281_362-276delinsAATATT	ENSP00000441861.1:n.362-281_362-276delins...
NM_000621.4:c.614-281_614-276delinsAATATT	NP_000612.1:n.614-281_614-276delinsAATATT...
NM_001165947.2:c.362-281_362-276delinsAATATT	NP_001159419.1:n.362-281_362-276delinsAAT...
NM_000621.5:c.614-281_614-276delinsAATATT MANE Select	NP_000612.1:n.614-281_614-276delinsAATATT...
NM_001165947.5:c.125-281_125-276delinsAATATT	NP_001159419.2:n.125-281_125-276delinsAAT...
NM_001378924.1:c.614-281_614-276delinsAATATT	NP_001365853.1:n.614-281_614-276delinsAAT...