Canonical Allele Identifier: CA656929826

Gene: HRH4

Linked Data

• COSMIC: COSN18741264

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24476600del , CM000680.2:g.24476600del	GRCh38
NC_000018.9:g.22056564del , CM000680.1:g.22056564del	GRCh37
NC_000018.8:g.20310562del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.358-147del MANE Select	ENSP00000256906.4:n.358-147del
ENST00000256906.4:c.358-147del	ENSP00000256906.4:n.358-147del
ENST00000426880.2:c.194-247del	ENSP00000402526.2:n.194-247del
NM_001143828.1:c.194-247del	NP_001137300.1:n.194-247del
NM_001160166.1:c.194-147del	NP_001153638.1:n.194-147del
NM_021624.3:c.358-147del	NP_067637.2:n.358-147del
XM_011526133.1:c.357+7649del	XP_011524435.1:n.357+7649del
NM_021624.4:c.358-147del MANE Select	NP_067637.2:n.358-147del
NM_001143828.2:c.194-247del	NP_001137300.1:n.194-247del
NM_001160166.2:c.194-147del	NP_001153638.1:n.194-147del