Canonical Allele Identifier: CA1948160642

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2445065G= , CM000673.2:g.2445065G=	GRCh38
NC_000011.9:g.2466295G= , CM000673.1:g.2466295G=	GRCh37
NC_000011.8:g.2422871G=	NCBI36
NG_008935.1:g.5075G= , LRG_287:g.5075G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.24-318G=	ENSP00000434560.2:n.24-318G=
ENST00000646564.2:c.-34G=	ENSP00000495806.2:n.-34G=
ENST00000155840.12:c.-34G= MANE Select	ENSP00000155840.2:n.-34G=
ENST00000155840.9:c.-34G=	ENSP00000155840.2:n.-34G=
ENST00000496887.6:c.24-318G=	ENSP00000434560.1:n.24-318G=
NM_000218.2:c.-34G= , LRG_287t1:c.-34G=	NP_000209.2:n.-34G=
NM_000218.3:c.-34G= MANE Select	NP_000209.2:n.-34G=