Canonical Allele Identifier: CA393084737

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73614856T>A (hg19) ; chr15:g.73322515T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322515T>A , CM000677.2:g.73322515T>A	GRCh38
NC_000015.9:g.73614856T>A , CM000677.1:g.73614856T>A	GRCh37
NC_000015.8:g.71401909T>A	NCBI36
NG_009063.1:g.51750A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3578A>T MANE Select	ENSP00000261917.3:p.Glu1193Val
ENST00000261917.3:c.3578A>T	ENSP00000261917.3:p.Glu1193Val
NM_005477.2:c.3578A>T	NP_005468.1:p.Glu1193Val
XM_011521148.1:c.2360A>T	XP_011519450.1:p.Glu787Val
XM_011521148.2:c.2360A>T	XP_011519450.1:p.Glu787Val
NM_005477.3:c.3578A>T MANE Select	NP_005468.1:p.Glu1193Val