Canonical Allele Identifier: CA1948225044
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2583519G= , CM000673.2:g.2583519G= GRCh38
NC_000011.9:g.2604749G= , CM000673.1:g.2604749G= GRCh37
NC_000011.8:g.2561325G= NCBI36
NG_008935.1:g.143529G= , LRG_287:g.143529G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.745G= ENSP00000434560.2:p.Ala249=
ENST00000646564.2:c.562G= ENSP00000495806.2:p.Ala188=
ENST00000155840.12:c.1006G= MANE Select ENSP00000155840.2:p.Ala336=
ENST00000335475.6:c.625G= ENSP00000334497.5:p.Ala209=
ENST00000646564.1:c.208G= ENSP00000495806.1:p.Ala70=
ENST00000155840.9:c.1006G= ENSP00000155840.2:p.Ala336=
ENST00000335475.5:c.625G= ENSP00000334497.5:p.Ala209=
NM_000218.2:c.1006G= , LRG_287t1:c.1006G= NP_000209.2:p.Ala336=
NM_181798.1:c.625G= , LRG_287t2:c.625G= NP_861463.1:p.Ala209=
NM_000218.3:c.1006G= MANE Select NP_000209.2:p.Ala336=