Canonical Allele Identifier: CA2575783821

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73322909del , CM000677.2:g.73322909del	GRCh38
NC_000015.9:g.73615250del , CM000677.1:g.73615250del	GRCh37
NC_000015.8:g.71402303del	NCBI36
NG_009063.1:g.51357del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.3185del MANE Select	ENSP00000261917.3:p.Pro1062HisfsTer?
ENST00000261917.3:c.3185del	ENSP00000261917.3:p.Pro1062HisfsTer?
NM_005477.2:c.3185del	NP_005468.1:p.Pro1062HisfsTer?
XM_011521148.1:c.1967del	XP_011519450.1:p.Pro656HisfsTer?
XM_011521148.2:c.1967del	XP_011519450.1:p.Pro656HisfsTer?
NM_005477.3:c.3185del MANE Select	NP_005468.1:p.Pro1062HisfsTer?