Canonical Allele Identifier: CA2187186366
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322646_73322647delinsGT , CM000677.2:g.73322646_73322647delinsGT GRCh38
NC_000015.9:g.73614987_73614988delinsGT , CM000677.1:g.73614987_73614988delinsGT GRCh37
NC_000015.8:g.71402040_71402041delinsGT NCBI36
NG_009063.1:g.51618_51619delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3446_3447delinsAC MANE Select ENSP00000261917.3:p.His1149=
ENST00000261917.3:c.3446_3447delinsAC ENSP00000261917.3:p.His1149=
NM_005477.2:c.3446_3447delinsAC NP_005468.1:p.His1149=
XM_011521148.1:c.2228_2229delinsAC XP_011519450.1:p.His743=
XM_011521148.2:c.2228_2229delinsAC XP_011519450.1:p.His743=
NM_005477.3:c.3446_3447delinsAC MANE Select NP_005468.1:p.His1149=
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