Canonical Allele Identifier: CA2576475331
Gene: HRH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24477209del , CM000680.2:g.24477209del GRCh38
NC_000018.9:g.22057173del , CM000680.1:g.22057173del GRCh37
NC_000018.8:g.20311171del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.820del MANE Select ENSP00000256906.4:p.Ser274ProfsTer12
ENST00000256906.4:c.820del ENSP00000256906.4:p.Ser274ProfsTer12
ENST00000426880.2:c.556del ENSP00000402526.2:p.Ser186ProfsTer12
NM_001143828.1:c.556del NP_001137300.1:p.Ser186ProfsTer12
NM_001160166.1:c.*452del NP_001153638.1:n.*452del
NM_021624.3:c.820del NP_067637.2:p.Ser274ProfsTer12
XM_011526133.1:c.357+8258del XP_011524435.1:n.357+8258del
NM_021624.4:c.820del MANE Select NP_067637.2:p.Ser274ProfsTer12
NM_001143828.2:c.556del NP_001137300.1:p.Ser186ProfsTer12
NM_001160166.2:c.*452del NP_001153638.1:n.*452del