Canonical Allele Identifier: CA1644352453

Gene: HTR1E

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.87015868C= , CM000668.2:g.87015868C=	GRCh38
NC_000006.11:g.87725586C= , CM000668.1:g.87725586C=	GRCh37
NC_000006.10:g.87782305C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000305344.7:c.534C= MANE Select	ENSP00000307766.4:p.Asp178=
ENST00000305344.6:c.534C=	ENSP00000307766.4:p.Asp178=
NM_000865.2:c.534C=	NP_000856.1:p.Asp178=
XM_011535789.1:c.534C=	XP_011534091.1:p.Asp178=
XM_011535790.1:c.534C=	XP_011534092.1:p.Asp178=
XM_011535789.2:c.534C=	XP_011534091.1:p.Asp178=
NM_000865.3:c.534C= MANE Select	NP_000856.1:p.Asp178=