Canonical Allele Identifier: CA1948224436

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2583369T= , CM000673.2:g.2583369T=	GRCh38
NC_000011.9:g.2604599T= , CM000673.1:g.2604599T=	GRCh37
NC_000011.8:g.2561175T=	NCBI36
NG_008935.1:g.143379T= , LRG_287:g.143379T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.661-66T=	ENSP00000434560.2:n.661-66T=
ENST00000646564.2:c.478-66T=	ENSP00000495806.2:n.478-66T=
ENST00000155840.12:c.922-66T= MANE Select	ENSP00000155840.2:n.922-66T=
ENST00000335475.6:c.541-66T=	ENSP00000334497.5:n.541-66T=
ENST00000646564.1:c.124-66T=	ENSP00000495806.1:n.124-66T=
ENST00000155840.9:c.922-66T=	ENSP00000155840.2:n.922-66T=
ENST00000335475.5:c.541-66T=	ENSP00000334497.5:n.541-66T=
NM_000218.2:c.922-66T= , LRG_287t1:c.922-66T=	NP_000209.2:n.922-66T=
NM_181798.1:c.541-66T= , LRG_287t2:c.541-66T=	NP_861463.1:n.541-66T=
NM_000218.3:c.922-66T= MANE Select	NP_000209.2:n.922-66T=