Canonical Allele Identifier: CA619410593

Gene: HCN4

Linked Data

• dbSNP Id: rs1255143771
• gnomAD v2: 15-73615062-AC-A
• gnomAD v4: 15-73322721-AC-A
• MyVariant Identifiers: chr15:g.73615063del (hg19) ; chr15:g.73322722del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322726del , CM000677.2:g.73322726del	GRCh38
NC_000015.9:g.73615067del , CM000677.1:g.73615067del	GRCh37
NC_000015.8:g.71402120del	NCBI36
NG_009063.1:g.51543del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3371del MANE Select	ENSP00000261917.3:p.Gly1124ValfsTer?
ENST00000261917.3:c.3371del	ENSP00000261917.3:p.Gly1124ValfsTer?
NM_005477.2:c.3371del	NP_005468.1:p.Gly1124ValfsTer?
XM_011521148.1:c.2153del	XP_011519450.1:p.Gly718ValfsTer?
XM_011521148.2:c.2153del	XP_011519450.1:p.Gly718ValfsTer?
NM_005477.3:c.3371del MANE Select	NP_005468.1:p.Gly1124ValfsTer?