Canonical Allele Identifier: CA491152538

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73624517T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73332176T>A , CM000677.2:g.73332176T>A	GRCh38
NC_000015.9:g.73624517T>A , CM000677.1:g.73624517T>A	GRCh37
NC_000015.8:g.71411570T>A	NCBI36
NG_009063.1:g.42089A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.1326A>T MANE Select	ENSP00000261917.3:p.Leu442=
ENST00000261917.3:c.1326A>T	ENSP00000261917.3:p.Leu442=
NM_005477.2:c.1326A>T	NP_005468.1:p.Leu442=
XM_011521148.1:c.108A>T	XP_011519450.1:p.Leu36=
XM_011521148.2:c.108A>T	XP_011519450.1:p.Leu36=
NM_005477.3:c.1326A>T MANE Select	NP_005468.1:p.Leu442=