Canonical Allele Identifier: CA811095263

Gene: HCN1

Linked Data

• dbSNP Id: rs1246726154
• MyVariant Identifiers: chr5:g.45461920_45461921del (hg19) ; chr5:g.45461818_45461819del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.45461820_45461821del , CM000667.2:g.45461820_45461821del	GRCh38
NC_000005.9:g.45461922_45461923del , CM000667.1:g.45461922_45461923del	GRCh37
NC_000005.8:g.45497679_45497680del	NCBI36
NG_042183.1:g.239300_239301del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303230.6:c.1011+27_1011+28del MANE Select	ENSP00000307342.4:n.1011+27_1011+28del
ENST00000637305.1:n.174+27_174+28del
ENST00000673735.1:c.1011+27_1011+28del	ENSP00000501107.1:n.1011+27_1011+28del
ENST00000303230.5:c.1011+27_1011+28del	ENSP00000307342.4:n.1011+27_1011+28del
NM_021072.3:c.1011+27_1011+28del	NP_066550.2:n.1011+27_1011+28del
NM_021072.4:c.1011+27_1011+28del MANE Select	NP_066550.2:n.1011+27_1011+28del