Canonical Allele Identifier: CA1948233033
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2587580G= , CM000673.2:g.2587580G= GRCh38
NC_000011.9:g.2608810G= , CM000673.1:g.2608810G= GRCh37
NC_000011.8:g.2565386G= NCBI36
NG_008935.1:g.147590G= , LRG_287:g.147590G=

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.782G= ENSP00000434560.2:p.Arg261=
ENST00000646564.2:c.599G= ENSP00000495806.2:p.Arg200=
ENST00000155840.12:c.1139G= MANE Select ENSP00000155840.2:p.Arg380=
ENST00000335475.6:c.758G= ENSP00000334497.5:p.Arg253=
ENST00000646564.1:c.245G= ENSP00000495806.1:p.Arg82=
ENST00000155840.9:c.1139G= ENSP00000155840.2:p.Arg380=
ENST00000335475.5:c.758G= ENSP00000334497.5:p.Arg253=
NM_000218.2:c.1139G= , LRG_287t1:c.1139G= NP_000209.2:p.Arg380=
NM_181798.1:c.758G= , LRG_287t2:c.758G= NP_861463.1:p.Arg253=
NM_000218.3:c.1139G= MANE Select NP_000209.2:p.Arg380=