Canonical Allele Identifier: CA1948315121

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2778024G= , CM000673.2:g.2778024G=	GRCh38
NC_000011.9:g.2799254G= , CM000673.1:g.2799254G=	GRCh37
NC_000011.8:g.2755830G=	NCBI36
NG_008935.1:g.338034G= , LRG_287:g.338034G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.1424G=	ENSP00000434560.2:p.Arg475=
ENST00000646564.2:c.1241G=	ENSP00000495806.2:p.Arg414=
ENST00000155840.12:c.1781G= MANE Select	ENSP00000155840.2:p.Arg594=
ENST00000335475.6:c.1400G=	ENSP00000334497.5:p.Arg467=
ENST00000526095.2:c.185G=	ENSP00000494939.1:p.Arg62=
ENST00000646564.1:c.887G=	ENSP00000495806.1:p.Arg296=
ENST00000155840.9:c.1781G=	ENSP00000155840.2:p.Arg594=
ENST00000335475.5:c.1400G=	ENSP00000334497.5:p.Arg467=
ENST00000526095.1:n.288G=
NM_000218.2:c.1781G= , LRG_287t1:c.1781G=	NP_000209.2:p.Arg594=
NM_181798.1:c.1400G= , LRG_287t2:c.1400G=	NP_861463.1:p.Arg467=
NM_000218.3:c.1781G= MANE Select	NP_000209.2:p.Arg594=