Canonical Allele Identifier: CA1948196715

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2527887G= , CM000673.2:g.2527887G=	GRCh38
NC_000011.9:g.2549117G= , CM000673.1:g.2549117G=	GRCh37
NC_000011.8:g.2505693G=	NCBI36
NG_008935.1:g.87897G= , LRG_287:g.87897G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000380776.5:n.184-41G=
ENST00000496887.7:c.126-41G=	ENSP00000434560.2:n.126-41G=
ENST00000646564.2:c.387-41G=	ENSP00000495806.2:n.387-41G=
ENST00000155840.12:c.387-41G= MANE Select	ENSP00000155840.2:n.387-41G=
ENST00000335475.6:c.6-41G=	ENSP00000334497.5:n.6-41G=
ENST00000646564.1:c.33-41G=	ENSP00000495806.1:n.33-41G=
ENST00000155840.9:c.387-41G=	ENSP00000155840.2:n.387-41G=
ENST00000335475.5:c.6-41G=	ENSP00000334497.5:n.6-41G=
ENST00000345015.4:n.256-41G=
ENST00000380776.4:c.177-41G=	ENSP00000370153.4:n.177-41G=
ENST00000496887.6:c.126-41G=	ENSP00000434560.1:n.126-41G=
NM_000218.2:c.387-41G= , LRG_287t1:c.387-41G=	NP_000209.2:n.387-41G=
NM_181798.1:c.6-41G= , LRG_287t2:c.6-41G=	NP_861463.1:n.6-41G=
NM_000218.3:c.387-41G= MANE Select	NP_000209.2:n.387-41G=