Canonical Allele Identifier: CA1948232780

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2587491G= , CM000673.2:g.2587491G=	GRCh38
NC_000011.9:g.2608721G= , CM000673.1:g.2608721G=	GRCh37
NC_000011.8:g.2565297G=	NCBI36
NG_008935.1:g.147501G= , LRG_287:g.147501G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.772-79G=	ENSP00000434560.2:n.772-79G=
ENST00000646564.2:c.589-79G=	ENSP00000495806.2:n.589-79G=
ENST00000155840.12:c.1129-79G= MANE Select	ENSP00000155840.2:n.1129-79G=
ENST00000335475.6:c.748-79G=	ENSP00000334497.5:n.748-79G=
ENST00000646564.1:c.235-79G=	ENSP00000495806.1:n.235-79G=
ENST00000155840.9:c.1129-79G=	ENSP00000155840.2:n.1129-79G=
ENST00000335475.5:c.748-79G=	ENSP00000334497.5:n.748-79G=
NM_000218.2:c.1129-79G= , LRG_287t1:c.1129-79G=	NP_000209.2:n.1129-79G=
NM_181798.1:c.748-79G= , LRG_287t2:c.748-79G=	NP_861463.1:n.748-79G=
NM_000218.3:c.1129-79G= MANE Select	NP_000209.2:n.1129-79G=