Canonical Allele Identifier: CA1948161021
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2445440C= , CM000673.2:g.2445440C= GRCh38
NC_000011.9:g.2466670C= , CM000673.1:g.2466670C= GRCh37
NC_000011.8:g.2423246C= NCBI36
NG_008935.1:g.5450C= , LRG_287:g.5450C=

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.81C= ENSP00000434560.2:p.Leu27=
ENST00000646564.2:c.342C= ENSP00000495806.2:p.Leu114=
ENST00000155840.12:c.342C= MANE Select ENSP00000155840.2:p.Leu114=
ENST00000155840.9:c.342C= ENSP00000155840.2:p.Leu114=
ENST00000345015.4:n.119C=
ENST00000496887.6:c.81C= ENSP00000434560.1:p.Leu27=
NM_000218.2:c.342C= , LRG_287t1:c.342C= NP_000209.2:p.Leu114=
NM_000218.3:c.342C= MANE Select NP_000209.2:p.Leu114=