Canonical Allele Identifier: CA2290577575

Gene: HRH4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24476822T= , CM000680.2:g.24476822T=	GRCh38
NC_000018.9:g.22056786T= , CM000680.1:g.22056786T=	GRCh37
NC_000018.8:g.20310784T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.433T= MANE Select	ENSP00000256906.4:p.Leu145=
ENST00000256906.4:c.433T=	ENSP00000256906.4:p.Leu145=
ENST00000426880.2:c.194-25T=	ENSP00000402526.2:n.194-25T=
NM_001143828.1:c.194-25T=	NP_001137300.1:n.194-25T=
NM_001160166.1:c.*65T=	NP_001153638.1:n.*65T=
NM_021624.3:c.433T=	NP_067637.2:p.Leu145=
XM_011526133.1:c.357+7871T=	XP_011524435.1:n.357+7871T=
NM_021624.4:c.433T= MANE Select	NP_067637.2:p.Leu145=
NM_001143828.2:c.194-25T=	NP_001137300.1:n.194-25T=
NM_001160166.2:c.*65T=	NP_001153638.1:n.*65T=