Canonical Allele Identifier: CA1948233040
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2587581G= , CM000673.2:g.2587581G= GRCh38
NC_000011.9:g.2608811G= , CM000673.1:g.2608811G= GRCh37
NC_000011.8:g.2565387G= NCBI36
NG_008935.1:g.147591G= , LRG_287:g.147591G=

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.783G= ENSP00000434560.2:p.Arg261=
ENST00000646564.2:c.600G= ENSP00000495806.2:p.Arg200=
ENST00000155840.12:c.1140G= MANE Select ENSP00000155840.2:p.Arg380=
ENST00000335475.6:c.759G= ENSP00000334497.5:p.Arg253=
ENST00000646564.1:c.246G= ENSP00000495806.1:p.Arg82=
ENST00000155840.9:c.1140G= ENSP00000155840.2:p.Arg380=
ENST00000335475.5:c.759G= ENSP00000334497.5:p.Arg253=
NM_000218.2:c.1140G= , LRG_287t1:c.1140G= NP_000209.2:p.Arg380=
NM_181798.1:c.759G= , LRG_287t2:c.759G= NP_861463.1:p.Arg253=
NM_000218.3:c.1140G= MANE Select NP_000209.2:p.Arg380=