Canonical Allele Identifier: CA1948171436

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2463484A= , CM000673.2:g.2463484A=	GRCh38
NC_000011.9:g.2484714A= , CM000673.1:g.2484714A=	GRCh37
NC_000011.8:g.2441290A=	NCBI36
NG_008935.1:g.23494A= , LRG_287:g.23494A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000380776.5:n.91+1507A=
ENST00000496887.7:c.125+18000A=	ENSP00000434560.2:n.125+18000A=
ENST00000646564.2:c.386+18000A=	ENSP00000495806.2:n.386+18000A=
ENST00000155840.12:c.386+18000A= MANE Select	ENSP00000155840.2:n.386+18000A=
ENST00000335475.6:c.5+1770A=	ENSP00000334497.5:n.5+1770A=
ENST00000646564.1:c.32+18000A=	ENSP00000495806.1:n.32+18000A=
ENST00000155840.9:c.386+18000A=	ENSP00000155840.2:n.386+18000A=
ENST00000335475.5:c.5+1770A=	ENSP00000334497.5:n.5+1770A=
ENST00000345015.4:n.163+18000A=
ENST00000380776.4:c.84+1507A=	ENSP00000370153.4:n.84+1507A=
ENST00000496887.6:c.125+18000A=	ENSP00000434560.1:n.125+18000A=
NM_000218.2:c.386+18000A= , LRG_287t1:c.386+18000A=	NP_000209.2:n.386+18000A=
NM_181798.1:c.5+1770A= , LRG_287t2:c.5+1770A=	NP_861463.1:n.5+1770A=
NM_000218.3:c.386+18000A= MANE Select	NP_000209.2:n.386+18000A=