Canonical Allele Identifier: CA619410591

Gene: HCN4

Linked Data

• dbSNP Id: rs2042867474
• gnomAD v2: 15-73614974-GAGGC-G
• MyVariant Identifiers: chr15:g.73614975_73614978del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322636_73322639del , CM000677.2:g.73322636_73322639del	GRCh38
NC_000015.9:g.73614977_73614980del , CM000677.1:g.73614977_73614980del	GRCh37
NC_000015.8:g.71402030_71402033del	NCBI36
NG_009063.1:g.51628_51631del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3456_3459del MANE Select	ENSP00000261917.3:p.Pro1153GlyfsTer27
ENST00000261917.3:c.3456_3459del	ENSP00000261917.3:p.Pro1153GlyfsTer27
NM_005477.2:c.3456_3459del	NP_005468.1:p.Pro1153GlyfsTer27
XM_011521148.1:c.2238_2241del	XP_011519450.1:p.Pro747GlyfsTer27
XM_011521148.2:c.2238_2241del	XP_011519450.1:p.Pro747GlyfsTer27
NM_005477.3:c.3456_3459del MANE Select	NP_005468.1:p.Pro1153GlyfsTer27