Canonical Allele Identifier: CA1948225508

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2583697G= , CM000673.2:g.2583697G=	GRCh38
NC_000011.9:g.2604927G= , CM000673.1:g.2604927G=	GRCh37
NC_000011.8:g.2561503G=	NCBI36
NG_008935.1:g.143707G= , LRG_287:g.143707G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.771+152G=	ENSP00000434560.2:n.771+152G=
ENST00000646564.2:c.588+152G=	ENSP00000495806.2:n.588+152G=
ENST00000155840.12:c.1032+152G= MANE Select	ENSP00000155840.2:n.1032+152G=
ENST00000335475.6:c.651+152G=	ENSP00000334497.5:n.651+152G=
ENST00000646564.1:c.234+152G=	ENSP00000495806.1:n.234+152G=
ENST00000155840.9:c.1032+152G=	ENSP00000155840.2:n.1032+152G=
ENST00000335475.5:c.651+152G=	ENSP00000334497.5:n.651+152G=
NM_000218.2:c.1032+152G= , LRG_287t1:c.1032+152G=	NP_000209.2:n.1032+152G=
NM_181798.1:c.651+152G= , LRG_287t2:c.651+152G=	NP_861463.1:n.651+152G=
NM_000218.3:c.1032+152G= MANE Select	NP_000209.2:n.1032+152G=