Canonical Allele Identifier: CA2187186847
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs2042870204

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322873_73322899del , CM000677.2:g.73322873_73322899del GRCh38
NC_000015.9:g.73615214_73615240del , CM000677.1:g.73615214_73615240del GRCh37
NC_000015.8:g.71402267_71402293del NCBI36
NG_009063.1:g.51368_51394del

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3196_3222del MANE Select ENSP00000261917.3:p.Pro1066_Leu1074del
ENST00000261917.3:c.3196_3222del ENSP00000261917.3:p.Pro1066_Leu1074del
NM_005477.2:c.3196_3222del NP_005468.1:p.Pro1066_Leu1074del
XM_011521148.1:c.1978_2004del XP_011519450.1:p.Pro660_Leu668del
XM_011521148.2:c.1978_2004del XP_011519450.1:p.Pro660_Leu668del
NM_005477.3:c.3196_3222del MANE Select NP_005468.1:p.Pro1066_Leu1074del