Canonical Allele Identifier: CA1948239501

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2570656C= , CM000673.2:g.2570656C=	GRCh38
NC_000011.9:g.2591886C= , CM000673.1:g.2591886C=	GRCh37
NC_000011.8:g.2548462C=	NCBI36
NG_008935.1:g.130666C= , LRG_287:g.130666C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.245C=	ENSP00000434560.2:p.Thr82=
ENST00000646564.2:c.478-12779C=	ENSP00000495806.2:n.478-12779C=
ENST00000155840.12:c.506C= MANE Select	ENSP00000155840.2:p.Thr169=
ENST00000335475.6:c.125C=	ENSP00000334497.5:p.Thr42=
ENST00000646564.1:c.124-12779C=	ENSP00000495806.1:n.124-12779C=
ENST00000155840.9:c.506C=	ENSP00000155840.2:p.Thr169=
ENST00000335475.5:c.125C=	ENSP00000334497.5:p.Thr42=
ENST00000496887.6:c.245C=	ENSP00000434560.1:p.Thr82=
NM_000218.2:c.506C= , LRG_287t1:c.506C=	NP_000209.2:p.Thr169=
NM_181798.1:c.125C= , LRG_287t2:c.125C=	NP_861463.1:p.Thr42=
NM_000218.3:c.506C= MANE Select	NP_000209.2:p.Thr169=