Canonical Allele Identifier: CA2811837915
Gene: HRH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476913_24476915dup , CM000680.2:g.24476913_24476915dup GRCh38
NC_000018.9:g.22056877_22056879dup , CM000680.1:g.22056877_22056879dup GRCh37
NC_000018.8:g.20310875_20310877dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.524_526dup MANE Select ENSP00000256906.4:p.Leu175_Ala176insVal
ENST00000256906.4:c.524_526dup ENSP00000256906.4:p.Leu175_Ala176insVal
ENST00000426880.2:c.260_262dup ENSP00000402526.2:p.Leu87_Ala88insVal
NM_001143828.1:c.260_262dup NP_001137300.1:p.Leu87_Ala88insVal
NM_001160166.1:c.*156_*158dup NP_001153638.1:n.*156_*158dup
NM_021624.3:c.524_526dup NP_067637.2:p.Leu175_Ala176insVal
XM_011526133.1:c.357+7962_357+7964dup XP_011524435.1:n.357+7962_357+7964dup
NM_021624.4:c.524_526dup MANE Select NP_067637.2:p.Leu175_Ala176insVal
NM_001143828.2:c.260_262dup NP_001137300.1:p.Leu87_Ala88insVal
NM_001160166.2:c.*156_*158dup NP_001153638.1:n.*156_*158dup