Canonical Allele Identifier: CA393085145
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322608G>A , CM000677.2:g.73322608G>A GRCh38
NC_000015.9:g.73614949G>A , CM000677.1:g.73614949G>A GRCh37
NC_000015.8:g.71402002G>A NCBI36
NG_009063.1:g.51657C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3485C>T MANE Select ENSP00000261917.3:p.Pro1162Leu
ENST00000261917.3:c.3485C>T ENSP00000261917.3:p.Pro1162Leu
NM_005477.2:c.3485C>T NP_005468.1:p.Pro1162Leu
XM_011521148.1:c.2267C>T XP_011519450.1:p.Pro756Leu
XM_011521148.2:c.2267C>T XP_011519450.1:p.Pro756Leu
NM_005477.3:c.3485C>T MANE Select NP_005468.1:p.Pro1162Leu