Canonical Allele Identifier: CA1948309960

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2768858A= , CM000673.2:g.2768858A=	GRCh38
NC_000011.9:g.2790088A= , CM000673.1:g.2790088A=	GRCh37
NC_000011.8:g.2746664A=	NCBI36
NG_008935.1:g.328868A= , LRG_287:g.328868A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1172A=	ENSP00000434560.2:p.His391=
ENST00000646564.2:c.989A=	ENSP00000495806.2:p.His330=
ENST00000155840.12:c.1529A= MANE Select	ENSP00000155840.2:p.His510=
ENST00000335475.6:c.1148A=	ENSP00000334497.5:p.His383=
ENST00000646564.1:c.635A=	ENSP00000495806.1:p.His212=
ENST00000155840.9:c.1529A=	ENSP00000155840.2:p.His510=
ENST00000335475.5:c.1148A=	ENSP00000334497.5:p.His383=
NM_000218.2:c.1529A= , LRG_287t1:c.1529A=	NP_000209.2:p.His510=
NM_181798.1:c.1148A= , LRG_287t2:c.1148A=	NP_861463.1:p.His383=
NM_000218.3:c.1529A= MANE Select	NP_000209.2:p.His510=