Canonical Allele Identifier: CA2629370538

Gene: HCN4

Linked Data

• gnomAD v4: 15-73322910-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322916dup , CM000677.2:g.73322916dup	GRCh38
NC_000015.9:g.73615257dup , CM000677.1:g.73615257dup	GRCh37
NC_000015.8:g.71402310dup	NCBI36
NG_009063.1:g.51354dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3182dup MANE Select	ENSP00000261917.3:p.Pro1062ThrfsTer?
ENST00000261917.3:c.3182dup	ENSP00000261917.3:p.Pro1062ThrfsTer?
NM_005477.2:c.3182dup	NP_005468.1:p.Pro1062ThrfsTer?
XM_011521148.1:c.1964dup	XP_011519450.1:p.Pro656ThrfsTer?
XM_011521148.2:c.1964dup	XP_011519450.1:p.Pro656ThrfsTer?
NM_005477.3:c.3182dup MANE Select	NP_005468.1:p.Pro1062ThrfsTer?