Canonical Allele Identifier: CA2580089981

Gene: HCN4

Linked Data

• ClinVar Variation Id: 2013419
• ClinVar RCV Id: RCV002856476

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323351del , CM000677.2:g.73323351del	GRCh38
NC_000015.9:g.73615692del , CM000677.1:g.73615692del	GRCh37
NC_000015.8:g.71402745del	NCBI36
NG_009063.1:g.50916del

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.2744del MANE Select	ENSP00000261917.3:p.Gly915ValfsTer?
ENST00000261917.3:c.2744del	ENSP00000261917.3:p.Gly915ValfsTer?
NM_005477.2:c.2744del	NP_005468.1:p.Gly915ValfsTer?
XM_011521148.1:c.1526del	XP_011519450.1:p.Gly509ValfsTer?
XM_011521148.2:c.1526del	XP_011519450.1:p.Gly509ValfsTer?
NM_005477.3:c.2744del MANE Select	NP_005468.1:p.Gly915ValfsTer?