Canonical Allele Identifier: CA1543688628

Gene: HCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45462122_45462123delinsTG , CM000667.2:g.45462122_45462123delinsTG	GRCh38
NC_000005.9:g.45462224_45462225delinsTG , CM000667.1:g.45462224_45462225delinsTG	GRCh37
NC_000005.8:g.45497981_45497982delinsTG	NCBI36
NG_042183.1:g.238996_238997delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303230.6:c.850-116_850-115delinsCA MANE Select	ENSP00000307342.4:n.850-116_850-115delinsCA
ENST00000637305.1:n.13-116_13-115delinsCA
ENST00000673735.1:c.850-116_850-115delinsCA	ENSP00000501107.1:n.850-116_850-115delinsCA
ENST00000303230.5:c.850-116_850-115delinsCA	ENSP00000307342.4:n.850-116_850-115delinsCA
NM_021072.3:c.850-116_850-115delinsCA	NP_066550.2:n.850-116_850-115delinsCA
NM_021072.4:c.850-116_850-115delinsCA MANE Select	NP_066550.2:n.850-116_850-115delinsCA