Canonical Allele Identifier: CA2574728206
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2583619C>A , CM000673.2:g.2583619C>A GRCh38
NC_000011.9:g.2604849C>A , CM000673.1:g.2604849C>A GRCh37
NC_000011.8:g.2561425C>A NCBI36
NG_008935.1:g.143629C>A , LRG_287:g.143629C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.771+74C>A ENSP00000434560.2:n.771+74C>A
ENST00000646564.2:c.588+74C>A ENSP00000495806.2:n.588+74C>A
ENST00000155840.12:c.1032+74C>A MANE Select ENSP00000155840.2:n.1032+74C>A
ENST00000335475.6:c.651+74C>A ENSP00000334497.5:n.651+74C>A
ENST00000646564.1:c.234+74C>A ENSP00000495806.1:n.234+74C>A
ENST00000155840.9:c.1032+74C>A ENSP00000155840.2:n.1032+74C>A
ENST00000335475.5:c.651+74C>A ENSP00000334497.5:n.651+74C>A
NM_000218.2:c.1032+74C>A , LRG_287t1:c.1032+74C>A NP_000209.2:n.1032+74C>A
NM_181798.1:c.651+74C>A , LRG_287t2:c.651+74C>A NP_861463.1:n.651+74C>A
NM_000218.3:c.1032+74C>A MANE Select NP_000209.2:n.1032+74C>A