Canonical Allele Identifier: CA1948228453
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2585074C= , CM000673.2:g.2585074C= GRCh38
NC_000011.9:g.2606304C= , CM000673.1:g.2606304C= GRCh37
NC_000011.8:g.2562880C= NCBI36
NG_008935.1:g.145084C= , LRG_287:g.145084C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.771+1529C= ENSP00000434560.2:n.771+1529C=
ENST00000646564.2:c.588+1529C= ENSP00000495806.2:n.588+1529C=
ENST00000155840.12:c.1033-138C= MANE Select ENSP00000155840.2:n.1033-138C=
ENST00000335475.6:c.652-138C= ENSP00000334497.5:n.652-138C=
ENST00000646564.1:c.234+1529C= ENSP00000495806.1:n.234+1529C=
ENST00000155840.9:c.1033-138C= ENSP00000155840.2:n.1033-138C=
ENST00000335475.5:c.652-138C= ENSP00000334497.5:n.652-138C=
NM_000218.2:c.1033-138C= , LRG_287t1:c.1033-138C= NP_000209.2:n.1033-138C=
NM_181798.1:c.652-138C= , LRG_287t2:c.652-138C= NP_861463.1:n.652-138C=
NM_000218.3:c.1033-138C= MANE Select NP_000209.2:n.1033-138C=