Canonical Allele Identifier: CA2187186506

Gene: HCN4

Linked Data

• dbSNP Id: rs1834958682

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322702_73322710del , CM000677.2:g.73322702_73322710del	GRCh38
NC_000015.9:g.73615043_73615051del , CM000677.1:g.73615043_73615051del	GRCh37
NC_000015.8:g.71402096_71402104del	NCBI36
NG_009063.1:g.51559_51567del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3387_3395del MANE Select	ENSP00000261917.3:p.Gly1130_Ser1132del
ENST00000261917.3:c.3387_3395del	ENSP00000261917.3:p.Gly1130_Ser1132del
NM_005477.2:c.3387_3395del	NP_005468.1:p.Gly1130_Ser1132del
XM_011521148.1:c.2169_2177del	XP_011519450.1:p.Gly724_Ser726del
XM_011521148.2:c.2169_2177del	XP_011519450.1:p.Gly724_Ser726del
NM_005477.3:c.3387_3395del MANE Select	NP_005468.1:p.Gly1130_Ser1132del