Canonical Allele Identifier: CA1948236529

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2588898T= , CM000673.2:g.2588898T=	GRCh38
NC_000011.9:g.2610128T= , CM000673.1:g.2610128T=	GRCh37
NC_000011.8:g.2566704T=	NCBI36
NG_008935.1:g.148908T= , LRG_287:g.148908T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1036+44T=	ENSP00000434560.2:n.1036+44T=
ENST00000646564.2:c.853+44T=	ENSP00000495806.2:n.853+44T=
ENST00000155840.12:c.1393+44T= MANE Select	ENSP00000155840.2:n.1393+44T=
ENST00000335475.6:c.1012+44T=	ENSP00000334497.5:n.1012+44T=
ENST00000646564.1:c.499+44T=	ENSP00000495806.1:n.499+44T=
ENST00000155840.9:c.1393+44T=	ENSP00000155840.2:n.1393+44T=
ENST00000335475.5:c.1012+44T=	ENSP00000334497.5:n.1012+44T=
NM_000218.2:c.1393+44T= , LRG_287t1:c.1393+44T=	NP_000209.2:n.1393+44T=
NM_181798.1:c.1012+44T= , LRG_287t2:c.1012+44T=	NP_861463.1:n.1012+44T=
NM_000218.3:c.1393+44T= MANE Select	NP_000209.2:n.1393+44T=