Canonical Allele Identifier: CA1948224412

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2583356T= , CM000673.2:g.2583356T=	GRCh38
NC_000011.9:g.2604586T= , CM000673.1:g.2604586T=	GRCh37
NC_000011.8:g.2561162T=	NCBI36
NG_008935.1:g.143366T= , LRG_287:g.143366T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.661-79T=	ENSP00000434560.2:n.661-79T=
ENST00000646564.2:c.478-79T=	ENSP00000495806.2:n.478-79T=
ENST00000155840.12:c.922-79T= MANE Select	ENSP00000155840.2:n.922-79T=
ENST00000335475.6:c.541-79T=	ENSP00000334497.5:n.541-79T=
ENST00000646564.1:c.124-79T=	ENSP00000495806.1:n.124-79T=
ENST00000155840.9:c.922-79T=	ENSP00000155840.2:n.922-79T=
ENST00000335475.5:c.541-79T=	ENSP00000334497.5:n.541-79T=
NM_000218.2:c.922-79T= , LRG_287t1:c.922-79T=	NP_000209.2:n.922-79T=
NM_181798.1:c.541-79T= , LRG_287t2:c.541-79T=	NP_861463.1:n.541-79T=
NM_000218.3:c.922-79T= MANE Select	NP_000209.2:n.922-79T=