Canonical Allele Identifier: CA1948161017
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2445430A= , CM000673.2:g.2445430A= GRCh38
NC_000011.9:g.2466660A= , CM000673.1:g.2466660A= GRCh37
NC_000011.8:g.2423236A= NCBI36
NG_008935.1:g.5440A= , LRG_287:g.5440A=

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.71A= ENSP00000434560.2:p.Tyr24=
ENST00000646564.2:c.332A= ENSP00000495806.2:p.Tyr111=
ENST00000155840.12:c.332A= MANE Select ENSP00000155840.2:p.Tyr111=
ENST00000155840.9:c.332A= ENSP00000155840.2:p.Tyr111=
ENST00000345015.4:n.109A=
ENST00000496887.6:c.71A= ENSP00000434560.1:p.Tyr24=
NM_000218.2:c.332A= , LRG_287t1:c.332A= NP_000209.2:p.Tyr111=
NM_000218.3:c.332A= MANE Select NP_000209.2:p.Tyr111=