Canonical Allele Identifier: CA619410587

Gene: HCN4

Linked Data

• dbSNP Id: rs1436490686
• gnomAD v2: 15-73614960-TGAG-T
• gnomAD v4: 15-73322619-TGAG-T
• MyVariant Identifiers: chr15:g.73614961_73614963del (hg19) ; chr15:g.73322620_73322622del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322622_73322624del , CM000677.2:g.73322622_73322624del	GRCh38
NC_000015.9:g.73614963_73614965del , CM000677.1:g.73614963_73614965del	GRCh37
NC_000015.8:g.71402016_71402018del	NCBI36
NG_009063.1:g.51643_51645del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3471_3473del MANE Select	ENSP00000261917.3:p.Ser1158del
ENST00000261917.3:c.3471_3473del	ENSP00000261917.3:p.Ser1158del
NM_005477.2:c.3471_3473del	NP_005468.1:p.Ser1158del
XM_011521148.1:c.2253_2255del	XP_011519450.1:p.Ser752del
XM_011521148.2:c.2253_2255del	XP_011519450.1:p.Ser752del
NM_005477.3:c.3471_3473del MANE Select	NP_005468.1:p.Ser1158del