Canonical Allele Identifier: CA491152535

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73624508G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73332167G>A , CM000677.2:g.73332167G>A	GRCh38
NC_000015.9:g.73624508G>A , CM000677.1:g.73624508G>A	GRCh37
NC_000015.8:g.71411561G>A	NCBI36
NG_009063.1:g.42098C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.1335C>T MANE Select	ENSP00000261917.3:p.Phe445=
ENST00000261917.3:c.1335C>T	ENSP00000261917.3:p.Phe445=
NM_005477.2:c.1335C>T	NP_005468.1:p.Phe445=
XM_011521148.1:c.117C>T	XP_011519450.1:p.Phe39=
XM_011521148.2:c.117C>T	XP_011519450.1:p.Phe39=
NM_005477.3:c.1335C>T MANE Select	NP_005468.1:p.Phe445=