Canonical Allele Identifier: CA1543688222
Gene: HCN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.45461844_45461845delinsAC , CM000667.2:g.45461844_45461845delinsAC GRCh38
NC_000005.9:g.45461946_45461947delinsAC , CM000667.1:g.45461946_45461947delinsAC GRCh37
NC_000005.8:g.45497703_45497704delinsAC NCBI36
NG_042183.1:g.239274_239275delinsGT

Transcript Alleles

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