Canonical Allele Identifier: CA1948229071
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2585275C= , CM000673.2:g.2585275C= GRCh38
NC_000011.9:g.2606505C= , CM000673.1:g.2606505C= GRCh37
NC_000011.8:g.2563081C= NCBI36
NG_008935.1:g.145285C= , LRG_287:g.145285C=

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.771+1730C= ENSP00000434560.2:n.771+1730C=
ENST00000646564.2:c.588+1730C= ENSP00000495806.2:n.588+1730C=
ENST00000155840.12:c.1096C= MANE Select ENSP00000155840.2:p.Arg366=
ENST00000335475.6:c.715C= ENSP00000334497.5:p.Arg239=
ENST00000646564.1:c.234+1730C= ENSP00000495806.1:n.234+1730C=
ENST00000155840.9:c.1096C= ENSP00000155840.2:p.Arg366=
ENST00000335475.5:c.715C= ENSP00000334497.5:p.Arg239=
NM_000218.2:c.1096C= , LRG_287t1:c.1096C= NP_000209.2:p.Arg366=
NM_181798.1:c.715C= , LRG_287t2:c.715C= NP_861463.1:p.Arg239=
NM_000218.3:c.1096C= MANE Select NP_000209.2:p.Arg366=