Canonical Allele Identifier: CA393093465
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329605G>T , CM000677.2:g.73329605G>T GRCh38
NC_000015.9:g.73621946G>T , CM000677.1:g.73621946G>T GRCh37
NC_000015.8:g.71408999G>T NCBI36
NG_009063.1:g.44660C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1558C>A MANE Select ENSP00000261917.3:p.Leu520Met
ENST00000261917.3:c.1558C>A ENSP00000261917.3:p.Leu520Met
NM_005477.2:c.1558C>A NP_005468.1:p.Leu520Met
XM_011521148.1:c.340C>A XP_011519450.1:p.Leu114Met
XM_011521148.2:c.340C>A XP_011519450.1:p.Leu114Met
NM_005477.3:c.1558C>A MANE Select NP_005468.1:p.Leu520Met