Canonical Allele Identifier: CA2641326619
Gene: HRH4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476633del , CM000680.2:g.24476633del GRCh38
NC_000018.9:g.22056597del , CM000680.1:g.22056597del GRCh37
NC_000018.8:g.20310595del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000256906.5:c.358-114del MANE Select ENSP00000256906.4:n.358-114del
ENST00000256906.4:c.358-114del ENSP00000256906.4:n.358-114del
ENST00000426880.2:c.194-214del ENSP00000402526.2:n.194-214del
NM_001143828.1:c.194-214del NP_001137300.1:n.194-214del
NM_001160166.1:c.194-114del NP_001153638.1:n.194-114del
NM_021624.3:c.358-114del NP_067637.2:n.358-114del
XM_011526133.1:c.357+7682del XP_011524435.1:n.357+7682del
NM_021624.4:c.358-114del MANE Select NP_067637.2:n.358-114del
NM_001143828.2:c.194-214del NP_001137300.1:n.194-214del
NM_001160166.2:c.194-114del NP_001153638.1:n.194-114del