Canonical Allele Identifier: CA1948315031

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2777862C= , CM000673.2:g.2777862C=	GRCh38
NC_000011.9:g.2799092C= , CM000673.1:g.2799092C=	GRCh37
NC_000011.8:g.2755668C=	NCBI36
NG_008935.1:g.337872C= , LRG_287:g.337872C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.1376-114C=	ENSP00000434560.2:n.1376-114C=
ENST00000646564.2:c.1193-114C=	ENSP00000495806.2:n.1193-114C=
ENST00000155840.12:c.1733-114C= MANE Select	ENSP00000155840.2:n.1733-114C=
ENST00000335475.6:c.1352-114C=	ENSP00000334497.5:n.1352-114C=
ENST00000526095.2:c.136+49C=	ENSP00000494939.1:n.136+49C=
ENST00000646564.1:c.839-114C=	ENSP00000495806.1:n.839-114C=
ENST00000155840.9:c.1733-114C=	ENSP00000155840.2:n.1733-114C=
ENST00000335475.5:c.1352-114C=	ENSP00000334497.5:n.1352-114C=
ENST00000526095.1:n.239+49C=
NM_000218.2:c.1733-114C= , LRG_287t1:c.1733-114C=	NP_000209.2:n.1733-114C=
NM_181798.1:c.1352-114C= , LRG_287t2:c.1352-114C=	NP_861463.1:n.1352-114C=
NM_000218.3:c.1733-114C= MANE Select	NP_000209.2:n.1733-114C=