Canonical Allele Identifier: CA2811837922
Gene: HRH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24477206del , CM000680.2:g.24477206del GRCh38
NC_000018.9:g.22057170del , CM000680.1:g.22057170del GRCh37
NC_000018.8:g.20311168del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.817del MANE Select ENSP00000256906.4:p.Ala273LeufsTer13
ENST00000256906.4:c.817del ENSP00000256906.4:p.Ala273LeufsTer13
ENST00000426880.2:c.553del ENSP00000402526.2:p.Ala185LeufsTer13
NM_001143828.1:c.553del NP_001137300.1:p.Ala185LeufsTer13
NM_001160166.1:c.*449del NP_001153638.1:n.*449del
NM_021624.3:c.817del NP_067637.2:p.Ala273LeufsTer13
XM_011526133.1:c.357+8255del XP_011524435.1:n.357+8255del
NM_021624.4:c.817del MANE Select NP_067637.2:p.Ala273LeufsTer13
NM_001143828.2:c.553del NP_001137300.1:p.Ala185LeufsTer13
NM_001160166.2:c.*449del NP_001153638.1:n.*449del