Canonical Allele Identifier: CA1948160581

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2445032G= , CM000673.2:g.2445032G=	GRCh38
NC_000011.9:g.2466262G= , CM000673.1:g.2466262G=	GRCh37
NC_000011.8:g.2422838G=	NCBI36
NG_008935.1:g.5042G= , LRG_287:g.5042G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.23+324G=	ENSP00000434560.2:n.23+324G=
ENST00000646564.2:c.-67G=	ENSP00000495806.2:n.-67G=
ENST00000155840.12:c.-67G= MANE Select	ENSP00000155840.2:n.-67G=
ENST00000155840.9:c.-67G=	ENSP00000155840.2:n.-67G=
ENST00000496887.6:c.23+324G=	ENSP00000434560.1:n.23+324G=
NM_000218.2:c.-67G= , LRG_287t1:c.-67G=	NP_000209.2:n.-67G=
NM_000218.3:c.-67G= MANE Select	NP_000209.2:n.-67G=