Canonical Allele Identifier: CA1948196642

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2527830T= , CM000673.2:g.2527830T=	GRCh38
NC_000011.9:g.2549060T= , CM000673.1:g.2549060T=	GRCh37
NC_000011.8:g.2505636T=	NCBI36
NG_008935.1:g.87840T= , LRG_287:g.87840T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380776.5:n.184-98T=
ENST00000496887.7:c.126-98T=	ENSP00000434560.2:n.126-98T=
ENST00000646564.2:c.387-98T=	ENSP00000495806.2:n.387-98T=
ENST00000155840.12:c.387-98T= MANE Select	ENSP00000155840.2:n.387-98T=
ENST00000335475.6:c.6-98T=	ENSP00000334497.5:n.6-98T=
ENST00000646564.1:c.33-98T=	ENSP00000495806.1:n.33-98T=
ENST00000155840.9:c.387-98T=	ENSP00000155840.2:n.387-98T=
ENST00000335475.5:c.6-98T=	ENSP00000334497.5:n.6-98T=
ENST00000345015.4:n.256-98T=
ENST00000380776.4:c.177-98T=	ENSP00000370153.4:n.177-98T=
ENST00000496887.6:c.126-98T=	ENSP00000434560.1:n.126-98T=
NM_000218.2:c.387-98T= , LRG_287t1:c.387-98T=	NP_000209.2:n.387-98T=
NM_181798.1:c.6-98T= , LRG_287t2:c.6-98T=	NP_861463.1:n.6-98T=
NM_000218.3:c.387-98T= MANE Select	NP_000209.2:n.387-98T=