Canonical Allele Identifier: CA1948236603

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2588923C= , CM000673.2:g.2588923C=	GRCh38
NC_000011.9:g.2610153C= , CM000673.1:g.2610153C=	GRCh37
NC_000011.8:g.2566729C=	NCBI36
NG_008935.1:g.148933C= , LRG_287:g.148933C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1036+69C=	ENSP00000434560.2:n.1036+69C=
ENST00000646564.2:c.853+69C=	ENSP00000495806.2:n.853+69C=
ENST00000155840.12:c.1393+69C= MANE Select	ENSP00000155840.2:n.1393+69C=
ENST00000335475.6:c.1012+69C=	ENSP00000334497.5:n.1012+69C=
ENST00000646564.1:c.499+69C=	ENSP00000495806.1:n.499+69C=
ENST00000155840.9:c.1393+69C=	ENSP00000155840.2:n.1393+69C=
ENST00000335475.5:c.1012+69C=	ENSP00000334497.5:n.1012+69C=
NM_000218.2:c.1393+69C= , LRG_287t1:c.1393+69C=	NP_000209.2:n.1393+69C=
NM_181798.1:c.1012+69C= , LRG_287t2:c.1012+69C=	NP_861463.1:n.1012+69C=
NM_000218.3:c.1393+69C= MANE Select	NP_000209.2:n.1393+69C=