Canonical Allele Identifier: CA1948309517

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2768465T= , CM000673.2:g.2768465T=	GRCh38
NC_000011.9:g.2789695T= , CM000673.1:g.2789695T=	GRCh37
NC_000011.8:g.2746271T=	NCBI36
NG_008935.1:g.328475T= , LRG_287:g.328475T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1158-379T=	ENSP00000434560.2:n.1158-379T=
ENST00000646564.2:c.975-379T=	ENSP00000495806.2:n.975-379T=
ENST00000155840.12:c.1515-379T= MANE Select	ENSP00000155840.2:n.1515-379T=
ENST00000335475.6:c.1134-379T=	ENSP00000334497.5:n.1134-379T=
ENST00000646564.1:c.621-379T=	ENSP00000495806.1:n.621-379T=
ENST00000155840.9:c.1515-379T=	ENSP00000155840.2:n.1515-379T=
ENST00000335475.5:c.1134-379T=	ENSP00000334497.5:n.1134-379T=
NM_000218.2:c.1515-379T= , LRG_287t1:c.1515-379T=	NP_000209.2:n.1515-379T=
NM_181798.1:c.1134-379T= , LRG_287t2:c.1134-379T=	NP_861463.1:n.1134-379T=
NM_000218.3:c.1515-379T= MANE Select	NP_000209.2:n.1515-379T=