Canonical Allele Identifier: CA1948242499
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2571981G= , CM000673.2:g.2571981G= GRCh38
NC_000011.9:g.2593211G= , CM000673.1:g.2593211G= GRCh37
NC_000011.8:g.2549787G= NCBI36
NG_008935.1:g.131991G= , LRG_287:g.131991G=

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.423-32G= ENSP00000434560.2:n.423-32G=
ENST00000646564.2:c.478-11454G= ENSP00000495806.2:n.478-11454G=
ENST00000155840.12:c.684-32G= MANE Select ENSP00000155840.2:n.684-32G=
ENST00000335475.6:c.303-32G= ENSP00000334497.5:n.303-32G=
ENST00000646564.1:c.124-11454G= ENSP00000495806.1:n.124-11454G=
ENST00000155840.9:c.684-32G= ENSP00000155840.2:n.684-32G=
ENST00000335475.5:c.303-32G= ENSP00000334497.5:n.303-32G=
ENST00000496887.6:c.423-32G= ENSP00000434560.1:n.423-32G=
NM_000218.2:c.684-32G= , LRG_287t1:c.684-32G= NP_000209.2:n.684-32G=
NM_181798.1:c.303-32G= , LRG_287t2:c.303-32G= NP_861463.1:n.303-32G=
NM_000218.3:c.684-32G= MANE Select NP_000209.2:n.684-32G=