Canonical Allele Identifier: CA1948212502

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2572993C= , CM000673.2:g.2572993C=	GRCh38
NC_000011.9:g.2594223C= , CM000673.1:g.2594223C=	GRCh37
NC_000011.8:g.2550799C=	NCBI36
NG_008935.1:g.133003C= , LRG_287:g.133003C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.660+7C=	ENSP00000434560.2:n.660+7C=
ENST00000646564.2:c.478-10442C=	ENSP00000495806.2:n.478-10442C=
ENST00000155840.12:c.921+7C= MANE Select	ENSP00000155840.2:n.921+7C=
ENST00000335475.6:c.540+7C=	ENSP00000334497.5:n.540+7C=
ENST00000646564.1:c.124-10442C=	ENSP00000495806.1:n.124-10442C=
ENST00000155840.9:c.921+7C=	ENSP00000155840.2:n.921+7C=
ENST00000335475.5:c.540+7C=	ENSP00000334497.5:n.540+7C=
NM_000218.2:c.921+7C= , LRG_287t1:c.921+7C=	NP_000209.2:n.921+7C=
NM_181798.1:c.540+7C= , LRG_287t2:c.540+7C=	NP_861463.1:n.540+7C=
NM_000218.3:c.921+7C= MANE Select	NP_000209.2:n.921+7C=