Canonical Allele Identifier: CA2290577726

Gene: HRH4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24477215_24477216delinsAT , CM000680.2:g.24477215_24477216delinsAT	GRCh38
NC_000018.9:g.22057179_22057180delinsAT , CM000680.1:g.22057179_22057180delinsAT	GRCh37
NC_000018.8:g.20311177_20311178delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.826_827delinsAT MANE Select	ENSP00000256906.4:p.Met276=
ENST00000256906.4:c.826_827delinsAT	ENSP00000256906.4:p.Met276=
ENST00000426880.2:c.562_563delinsAT	ENSP00000402526.2:p.Met188=
NM_001143828.1:c.562_563delinsAT	NP_001137300.1:p.Met188=
NM_001160166.1:c.*458_*459delinsAT	NP_001153638.1:n.*458_*459delinsAT
NM_021624.3:c.826_827delinsAT	NP_067637.2:p.Met276=
XM_011526133.1:c.357+8264_357+8265delinsAT	XP_011524435.1:n.357+8264_357+8265delinsAT
NM_021624.4:c.826_827delinsAT MANE Select	NP_067637.2:p.Met276=
NM_001143828.2:c.562_563delinsAT	NP_001137300.1:p.Met188=
NM_001160166.2:c.*458_*459delinsAT	NP_001153638.1:n.*458_*459delinsAT