Canonical Allele Identifier: CA1948228991

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2585258G= , CM000673.2:g.2585258G=	GRCh38
NC_000011.9:g.2606488G= , CM000673.1:g.2606488G=	GRCh37
NC_000011.8:g.2563064G=	NCBI36
NG_008935.1:g.145268G= , LRG_287:g.145268G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.771+1713G=	ENSP00000434560.2:n.771+1713G=
ENST00000646564.2:c.588+1713G=	ENSP00000495806.2:n.588+1713G=
ENST00000155840.12:c.1079G= MANE Select	ENSP00000155840.2:p.Arg360=
ENST00000335475.6:c.698G=	ENSP00000334497.5:p.Arg233=
ENST00000646564.1:c.234+1713G=	ENSP00000495806.1:n.234+1713G=
ENST00000155840.9:c.1079G=	ENSP00000155840.2:p.Arg360=
ENST00000335475.5:c.698G=	ENSP00000334497.5:p.Arg233=
NM_000218.2:c.1079G= , LRG_287t1:c.1079G=	NP_000209.2:p.Arg360=
NM_181798.1:c.698G= , LRG_287t2:c.698G=	NP_861463.1:p.Arg233=
NM_000218.3:c.1079G= MANE Select	NP_000209.2:p.Arg360=