Canonical Allele Identifier: CA393098981

Gene: HCN4

Linked Data

• dbSNP Id: rs753874425
• gnomAD v4: 15-73368154-G-GC
• MyVariant Identifiers: chr15:g.73660495_73660496insC (hg19) ; chr15:g.73368154_73368155insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73368159dup , CM000677.2:g.73368159dup	GRCh38
NC_000015.9:g.73660500dup , CM000677.1:g.73660500dup	GRCh37
NC_000015.8:g.71447553dup	NCBI36
NG_009063.1:g.6110dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.116dup MANE Select	ENSP00000261917.3:p.Arg40ProfsTer?
ENST00000261917.3:c.116dup	ENSP00000261917.3:p.Arg40ProfsTer?
NM_005477.2:c.116dup	NP_005468.1:p.Arg40ProfsTer?
NM_005477.3:c.116dup MANE Select	NP_005468.1:p.Arg40ProfsTer?