Canonical Allele Identifier: CA2290577699

Gene: HRH4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24477138_24477140delinsCAG , CM000680.2:g.24477138_24477140delinsCAG	GRCh38
NC_000018.9:g.22057102_22057104delinsCAG , CM000680.1:g.22057102_22057104delinsCAG	GRCh37
NC_000018.8:g.20311100_20311102delinsCAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.749_751delinsCAG MANE Select	ENSP00000256906.4:p.Ser250=
ENST00000256906.4:c.749_751delinsCAG	ENSP00000256906.4:p.Ser250=
ENST00000426880.2:c.485_487delinsCAG	ENSP00000402526.2:p.Ser162=
NM_001143828.1:c.485_487delinsCAG	NP_001137300.1:p.Ser162=
NM_001160166.1:c.*381_*383delinsCAG	NP_001153638.1:n.*381_*383delinsCAG
NM_021624.3:c.749_751delinsCAG	NP_067637.2:p.Ser250=
XM_011526133.1:c.357+8187_357+8189delinsCAG	XP_011524435.1:n.357+8187_357+8189delinsCAG
NM_021624.4:c.749_751delinsCAG MANE Select	NP_067637.2:p.Ser250=
NM_001143828.2:c.485_487delinsCAG	NP_001137300.1:p.Ser162=
NM_001160166.2:c.*381_*383delinsCAG	NP_001153638.1:n.*381_*383delinsCAG