Canonical Allele Identifier: CA393093541

Gene: HCN4

Linked Data

• COSMIC: COSM6419535
• MyVariant Identifiers: chr15:g.73621964T>C (hg19) ; chr15:g.73329623T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73329623T>C , CM000677.2:g.73329623T>C	GRCh38
NC_000015.9:g.73621964T>C , CM000677.1:g.73621964T>C	GRCh37
NC_000015.8:g.71409017T>C	NCBI36
NG_009063.1:g.44642A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.1540A>G MANE Select	ENSP00000261917.3:p.Thr514Ala
ENST00000261917.3:c.1540A>G	ENSP00000261917.3:p.Thr514Ala
NM_005477.2:c.1540A>G	NP_005468.1:p.Thr514Ala
XM_011521148.1:c.322A>G	XP_011519450.1:p.Thr108Ala
XM_011521148.2:c.322A>G	XP_011519450.1:p.Thr108Ala
NM_005477.3:c.1540A>G MANE Select	NP_005468.1:p.Thr514Ala