Canonical Allele Identifier: CA2290577713

Gene: HRH4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24477176_24477177delinsTC , CM000680.2:g.24477176_24477177delinsTC	GRCh38
NC_000018.9:g.22057140_22057141delinsTC , CM000680.1:g.22057140_22057141delinsTC	GRCh37
NC_000018.8:g.20311138_20311139delinsTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.787_788delinsTC MANE Select	ENSP00000256906.4:p.Ser263=
ENST00000256906.4:c.787_788delinsTC	ENSP00000256906.4:p.Ser263=
ENST00000426880.2:c.523_524delinsTC	ENSP00000402526.2:p.Ser175=
NM_001143828.1:c.523_524delinsTC	NP_001137300.1:p.Ser175=
NM_001160166.1:c.*419_*420delinsTC	NP_001153638.1:n.*419_*420delinsTC
NM_021624.3:c.787_788delinsTC	NP_067637.2:p.Ser263=
XM_011526133.1:c.357+8225_357+8226delinsTC	XP_011524435.1:n.357+8225_357+8226delinsTC
NM_021624.4:c.787_788delinsTC MANE Select	NP_067637.2:p.Ser263=
NM_001143828.2:c.523_524delinsTC	NP_001137300.1:p.Ser175=
NM_001160166.2:c.*419_*420delinsTC	NP_001153638.1:n.*419_*420delinsTC