Canonical Allele Identifier: CA393086161
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322966G>C , CM000677.2:g.73322966G>C GRCh38
NC_000015.9:g.73615307G>C , CM000677.1:g.73615307G>C GRCh37
NC_000015.8:g.71402360G>C NCBI36
NG_009063.1:g.51299C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3127C>G MANE Select ENSP00000261917.3:p.Pro1043Ala
ENST00000261917.3:c.3127C>G ENSP00000261917.3:p.Pro1043Ala
NM_005477.2:c.3127C>G NP_005468.1:p.Pro1043Ala
XM_011521148.1:c.1909C>G XP_011519450.1:p.Pro637Ala
XM_011521148.2:c.1909C>G XP_011519450.1:p.Pro637Ala
NM_005477.3:c.3127C>G MANE Select NP_005468.1:p.Pro1043Ala