Canonical Allele Identifier: CA393085568
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322759A>G , CM000677.2:g.73322759A>G GRCh38
NC_000015.9:g.73615100A>G , CM000677.1:g.73615100A>G GRCh37
NC_000015.8:g.71402153A>G NCBI36
NG_009063.1:g.51506T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3334T>C MANE Select ENSP00000261917.3:p.Ser1112Pro
ENST00000261917.3:c.3334T>C ENSP00000261917.3:p.Ser1112Pro
NM_005477.2:c.3334T>C NP_005468.1:p.Ser1112Pro
XM_011521148.1:c.2116T>C XP_011519450.1:p.Ser706Pro
XM_011521148.2:c.2116T>C XP_011519450.1:p.Ser706Pro
NM_005477.3:c.3334T>C MANE Select NP_005468.1:p.Ser1112Pro