Canonical Allele Identifier: CA1948225138
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2583538T= , CM000673.2:g.2583538T= GRCh38
NC_000011.9:g.2604768T= , CM000673.1:g.2604768T= GRCh37
NC_000011.8:g.2561344T= NCBI36
NG_008935.1:g.143548T= , LRG_287:g.143548T=

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.764T= ENSP00000434560.2:p.Leu255=
ENST00000646564.2:c.581T= ENSP00000495806.2:p.Leu194=
ENST00000155840.12:c.1025T= MANE Select ENSP00000155840.2:p.Leu342=
ENST00000335475.6:c.644T= ENSP00000334497.5:p.Leu215=
ENST00000646564.1:c.227T= ENSP00000495806.1:p.Leu76=
ENST00000155840.9:c.1025T= ENSP00000155840.2:p.Leu342=
ENST00000335475.5:c.644T= ENSP00000334497.5:p.Leu215=
NM_000218.2:c.1025T= , LRG_287t1:c.1025T= NP_000209.2:p.Leu342=
NM_181798.1:c.644T= , LRG_287t2:c.644T= NP_861463.1:p.Leu215=
NM_000218.3:c.1025T= MANE Select NP_000209.2:p.Leu342=