Canonical Allele Identifier: CA2290577711

Gene: HRH4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24477170T= , CM000680.2:g.24477170T=	GRCh38
NC_000018.9:g.22057134T= , CM000680.1:g.22057134T=	GRCh37
NC_000018.8:g.20311132T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.781T= MANE Select	ENSP00000256906.4:p.Phe261=
ENST00000256906.4:c.781T=	ENSP00000256906.4:p.Phe261=
ENST00000426880.2:c.517T=	ENSP00000402526.2:p.Phe173=
NM_001143828.1:c.517T=	NP_001137300.1:p.Phe173=
NM_001160166.1:c.*413T=	NP_001153638.1:n.*413T=
NM_021624.3:c.781T=	NP_067637.2:p.Phe261=
XM_011526133.1:c.357+8219T=	XP_011524435.1:n.357+8219T=
NM_021624.4:c.781T= MANE Select	NP_067637.2:p.Phe261=
NM_001143828.2:c.517T=	NP_001137300.1:p.Phe173=
NM_001160166.2:c.*413T=	NP_001153638.1:n.*413T=