Canonical Allele Identifier: CA2839758933
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323769del , CM000677.2:g.73323769del GRCh38
NC_000015.9:g.73616110del , CM000677.1:g.73616110del GRCh37
NC_000015.8:g.71403163del NCBI36
NG_009063.1:g.50499del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2327del MANE Select ENSP00000261917.3:p.Pro776ArgfsTer2
ENST00000261917.3:c.2327del ENSP00000261917.3:p.Pro776ArgfsTer2
NM_005477.2:c.2327del NP_005468.1:p.Pro776ArgfsTer2
XM_011521148.1:c.1109del XP_011519450.1:p.Pro370ArgfsTer2
XM_011521148.2:c.1109del XP_011519450.1:p.Pro370ArgfsTer2
NM_005477.3:c.2327del MANE Select NP_005468.1:p.Pro776ArgfsTer2
Search 100 bp 5'
Search 100 bp 3'