Canonical Allele Identifier: CA1543790829

Gene: HCN1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45645612_45645616delinsCAACA , CM000667.2:g.45645612_45645616delinsCAACA	GRCh38
NC_000005.9:g.45645714_45645718delinsCAACA , CM000667.1:g.45645714_45645718delinsCAACA	GRCh37
NC_000005.8:g.45681471_45681475delinsCAACA	NCBI36
NG_042183.1:g.55503_55507delinsTGTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303230.6:c.426-8_426-4delinsTGTTG MANE Select	ENSP00000307342.4:n.426-8_426-4delinsTGTTG
ENST00000673735.1:c.426-8_426-4delinsTGTTG	ENSP00000501107.1:n.426-8_426-4delinsTGTTG
ENST00000303230.5:c.426-8_426-4delinsTGTTG	ENSP00000307342.4:n.426-8_426-4delinsTGTTG
ENST00000634658.1:c.426-8_426-4delinsTGTTG	ENSP00000489134.1:n.426-8_426-4delinsTGTTG
NM_021072.3:c.426-8_426-4delinsTGTTG	NP_066550.2:n.426-8_426-4delinsTGTTG
NM_021072.4:c.426-8_426-4delinsTGTTG MANE Select	NP_066550.2:n.426-8_426-4delinsTGTTG