Canonical Allele Identifier: CA1948196605

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2527789T= , CM000673.2:g.2527789T=	GRCh38
NC_000011.9:g.2549019T= , CM000673.1:g.2549019T=	GRCh37
NC_000011.8:g.2505595T=	NCBI36
NG_008935.1:g.87799T= , LRG_287:g.87799T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380776.5:n.184-139T=
ENST00000496887.7:c.126-139T=	ENSP00000434560.2:n.126-139T=
ENST00000646564.2:c.387-139T=	ENSP00000495806.2:n.387-139T=
ENST00000155840.12:c.387-139T= MANE Select	ENSP00000155840.2:n.387-139T=
ENST00000335475.6:c.6-139T=	ENSP00000334497.5:n.6-139T=
ENST00000646564.1:c.33-139T=	ENSP00000495806.1:n.33-139T=
ENST00000155840.9:c.387-139T=	ENSP00000155840.2:n.387-139T=
ENST00000335475.5:c.6-139T=	ENSP00000334497.5:n.6-139T=
ENST00000345015.4:n.256-139T=
ENST00000380776.4:c.177-139T=	ENSP00000370153.4:n.177-139T=
ENST00000496887.6:c.126-139T=	ENSP00000434560.1:n.126-139T=
NM_000218.2:c.387-139T= , LRG_287t1:c.387-139T=	NP_000209.2:n.387-139T=
NM_181798.1:c.6-139T= , LRG_287t2:c.6-139T=	NP_861463.1:n.6-139T=
NM_000218.3:c.387-139T= MANE Select	NP_000209.2:n.387-139T=