Canonical Allele Identifier: CA2187194540
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367758_73367767delinsTGGCTGCTGG , CM000677.2:g.73367758_73367767delinsTGGCTGCTGG GRCh38
NC_000015.9:g.73660099_73660108delinsTGGCTGCTGG , CM000677.1:g.73660099_73660108delinsTGGCTGCTGG GRCh37
NC_000015.8:g.71447152_71447161delinsTGGCTGCTGG NCBI36
NG_009063.1:g.6498_6507delinsCCAGCAGCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.504_513delinsCCAGCAGCCA MANE Select ENSP00000261917.3:p.Pro168=
ENST00000261917.3:c.504_513delinsCCAGCAGCCA ENSP00000261917.3:p.Pro168=
NM_005477.2:c.504_513delinsCCAGCAGCCA NP_005468.1:p.Pro168=
NM_005477.3:c.504_513delinsCCAGCAGCCA MANE Select NP_005468.1:p.Pro168=
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