Canonical Allele Identifier: CA2187188881

Gene: HCN4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323983_73323990delinsAGAGCGGG , CM000677.2:g.73323983_73323990delinsAGAGCGGG	GRCh38
NC_000015.9:g.73616324_73616331delinsAGAGCGGG , CM000677.1:g.73616324_73616331delinsAGAGCGGG	GRCh37
NC_000015.8:g.71403377_71403384delinsAGAGCGGG	NCBI36
NG_009063.1:g.50275_50282delinsCCCGCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261917.4:c.2144-41_2144-34delinsCCCGCTCT MANE Select	ENSP00000261917.3:n.2144-41_2144-34delinsCCCGCTCT
ENST00000261917.3:c.2144-41_2144-34delinsCCCGCTCT	ENSP00000261917.3:n.2144-41_2144-34delinsCCCGCTCT
NM_005477.2:c.2144-41_2144-34delinsCCCGCTCT	NP_005468.1:n.2144-41_2144-34delinsCCCGCTCT
XM_011521148.1:c.926-41_926-34delinsCCCGCTCT	XP_011519450.1:n.926-41_926-34delinsCCCGCTCT
XM_011521148.2:c.926-41_926-34delinsCCCGCTCT	XP_011519450.1:n.926-41_926-34delinsCCCGCTCT
NM_005477.3:c.2144-41_2144-34delinsCCCGCTCT MANE Select	NP_005468.1:n.2144-41_2144-34delinsCCCGCTCT