Canonical Allele Identifier: CA2575784037

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73368214_73368215insG , CM000677.2:g.73368214_73368215insG	GRCh38
NC_000015.9:g.73660555_73660556insG , CM000677.1:g.73660555_73660556insG	GRCh37
NC_000015.8:g.71447608_71447609insG	NCBI36
NG_009063.1:g.6050_6051insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.56_57insC MANE Select	ENSP00000261917.3:p.Ala21GlyfsTer?
ENST00000261917.3:c.56_57insC	ENSP00000261917.3:p.Ala21GlyfsTer?
NM_005477.2:c.56_57insC	NP_005468.1:p.Ala21GlyfsTer?
NM_005477.3:c.56_57insC MANE Select	NP_005468.1:p.Ala21GlyfsTer?