Canonical Allele Identifier: CA2187187029
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322936G= , CM000677.2:g.73322936G= GRCh38
NC_000015.9:g.73615277G= , CM000677.1:g.73615277G= GRCh37
NC_000015.8:g.71402330G= NCBI36
NG_009063.1:g.51329C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3157C= MANE Select ENSP00000261917.3:p.Leu1053=
ENST00000261917.3:c.3157C= ENSP00000261917.3:p.Leu1053=
NM_005477.2:c.3157C= NP_005468.1:p.Leu1053=
XM_011521148.1:c.1939C= XP_011519450.1:p.Leu647=
XM_011521148.2:c.1939C= XP_011519450.1:p.Leu647=
NM_005477.3:c.3157C= MANE Select NP_005468.1:p.Leu1053=