Canonical Allele Identifier: CA393093675

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73621991A>T (hg19) ; chr15:g.73329650A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73329650A>T , CM000677.2:g.73329650A>T	GRCh38
NC_000015.9:g.73621991A>T , CM000677.1:g.73621991A>T	GRCh37
NC_000015.8:g.71409044A>T	NCBI36
NG_009063.1:g.44615T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1513T>A MANE Select	ENSP00000261917.3:p.Cys505Ser
ENST00000261917.3:c.1513T>A	ENSP00000261917.3:p.Cys505Ser
NM_005477.2:c.1513T>A	NP_005468.1:p.Cys505Ser
XM_011521148.1:c.295T>A	XP_011519450.1:p.Cys99Ser
XM_011521148.2:c.295T>A	XP_011519450.1:p.Cys99Ser
NM_005477.3:c.1513T>A MANE Select	NP_005468.1:p.Cys505Ser