Canonical Allele Identifier: CA2290577584
Gene: HRH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476840_24476847delinsATTCTAGT , CM000680.2:g.24476840_24476847delinsATTCTAGT GRCh38
NC_000018.9:g.22056804_22056811delinsATTCTAGT , CM000680.1:g.22056804_22056811delinsATTCTAGT GRCh37
NC_000018.8:g.20310802_20310809delinsATTCTAGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.451_458delinsATTCTAGT MANE Select ENSP00000256906.4:p.Ile151=
ENST00000256906.4:c.451_458delinsATTCTAGT ENSP00000256906.4:p.Ile151=
ENST00000426880.2:c.194-7_194delinsATTCTAGT
NM_001143828.1:c.194-7_194delinsATTCTAGT
NM_001160166.1:c.*83_*90delinsATTCTAGT NP_001153638.1:n.*83_*90delinsATTCTAGT
NM_021624.3:c.451_458delinsATTCTAGT NP_067637.2:p.Ile151=
XM_011526133.1:c.357+7889_357+7896delinsATTCTAGT XP_011524435.1:n.357+7889_357+7896delinsATTCTAGT
NM_021624.4:c.451_458delinsATTCTAGT MANE Select NP_067637.2:p.Ile151=
NM_001143828.2:c.194-7_194delinsATTCTAGT
NM_001160166.2:c.*83_*90delinsATTCTAGT NP_001153638.1:n.*83_*90delinsATTCTAGT