Canonical Allele Identifier: CA1948225616

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2583787T= , CM000673.2:g.2583787T=	GRCh38
NC_000011.9:g.2605017T= , CM000673.1:g.2605017T=	GRCh37
NC_000011.8:g.2561593T=	NCBI36
NG_008935.1:g.143797T= , LRG_287:g.143797T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.771+242T=	ENSP00000434560.2:n.771+242T=
ENST00000646564.2:c.588+242T=	ENSP00000495806.2:n.588+242T=
ENST00000155840.12:c.1032+242T= MANE Select	ENSP00000155840.2:n.1032+242T=
ENST00000335475.6:c.651+242T=	ENSP00000334497.5:n.651+242T=
ENST00000646564.1:c.234+242T=	ENSP00000495806.1:n.234+242T=
ENST00000155840.9:c.1032+242T=	ENSP00000155840.2:n.1032+242T=
ENST00000335475.5:c.651+242T=	ENSP00000334497.5:n.651+242T=
NM_000218.2:c.1032+242T= , LRG_287t1:c.1032+242T=	NP_000209.2:n.1032+242T=
NM_181798.1:c.651+242T= , LRG_287t2:c.651+242T=	NP_861463.1:n.651+242T=
NM_000218.3:c.1032+242T= MANE Select	NP_000209.2:n.1032+242T=