Canonical Allele Identifier: CA2290577731

Gene: HRH4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24477232_24477233delinsAT , CM000680.2:g.24477232_24477233delinsAT	GRCh38
NC_000018.9:g.22057196_22057197delinsAT , CM000680.1:g.22057196_22057197delinsAT	GRCh37
NC_000018.8:g.20311194_20311195delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.843_844delinsAT MANE Select	ENSP00000256906.4:p.Gln281=
ENST00000256906.4:c.843_844delinsAT	ENSP00000256906.4:p.Gln281=
ENST00000426880.2:c.579_580delinsAT	ENSP00000402526.2:p.Gln193=
NM_001143828.1:c.579_580delinsAT	NP_001137300.1:p.Gln193=
NM_001160166.1:c.*475_*476delinsAT	NP_001153638.1:n.*475_*476delinsAT
NM_021624.3:c.843_844delinsAT	NP_067637.2:p.Gln281=
XM_011526133.1:c.357+8281_357+8282delinsAT	XP_011524435.1:n.357+8281_357+8282delinsAT
NM_021624.4:c.843_844delinsAT MANE Select	NP_067637.2:p.Gln281=
NM_001143828.2:c.579_580delinsAT	NP_001137300.1:p.Gln193=
NM_001160166.2:c.*475_*476delinsAT	NP_001153638.1:n.*475_*476delinsAT