Canonical Allele Identifier: CA393085333
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322660T>G , CM000677.2:g.73322660T>G GRCh38
NC_000015.9:g.73615001T>G , CM000677.1:g.73615001T>G GRCh37
NC_000015.8:g.71402054T>G NCBI36
NG_009063.1:g.51605A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3433A>C MANE Select ENSP00000261917.3:p.Ile1145Leu
ENST00000261917.3:c.3433A>C ENSP00000261917.3:p.Ile1145Leu
NM_005477.2:c.3433A>C NP_005468.1:p.Ile1145Leu
XM_011521148.1:c.2215A>C XP_011519450.1:p.Ile739Leu
XM_011521148.2:c.2215A>C XP_011519450.1:p.Ile739Leu
NM_005477.3:c.3433A>C MANE Select NP_005468.1:p.Ile1145Leu