Canonical Allele Identifier: CA2290577473
Gene: HRH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476639_24476640delinsTA , CM000680.2:g.24476639_24476640delinsTA GRCh38
NC_000018.9:g.22056603_22056604delinsTA , CM000680.1:g.22056603_22056604delinsTA GRCh37
NC_000018.8:g.20310601_20310602delinsTA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000256906.5:c.358-108_358-107delinsTA MANE Select ENSP00000256906.4:n.358-108_358-107delinsTA
ENST00000256906.4:c.358-108_358-107delinsTA ENSP00000256906.4:n.358-108_358-107delinsTA
ENST00000426880.2:c.194-208_194-207delinsTA ENSP00000402526.2:n.194-208_194-207delinsTA
NM_001143828.1:c.194-208_194-207delinsTA NP_001137300.1:n.194-208_194-207delinsTA
NM_001160166.1:c.194-108_194-107delinsTA NP_001153638.1:n.194-108_194-107delinsTA
NM_021624.3:c.358-108_358-107delinsTA NP_067637.2:n.358-108_358-107delinsTA
XM_011526133.1:c.357+7688_357+7689delinsTA XP_011524435.1:n.357+7688_357+7689delinsTA
NM_021624.4:c.358-108_358-107delinsTA MANE Select NP_067637.2:n.358-108_358-107delinsTA
NM_001143828.2:c.194-208_194-207delinsTA NP_001137300.1:n.194-208_194-207delinsTA
NM_001160166.2:c.194-108_194-107delinsTA NP_001153638.1:n.194-108_194-107delinsTA