Canonical Allele Identifier: CA1948239580

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2570665T= , CM000673.2:g.2570665T=	GRCh38
NC_000011.9:g.2591895T= , CM000673.1:g.2591895T=	GRCh37
NC_000011.8:g.2548471T=	NCBI36
NG_008935.1:g.130675T= , LRG_287:g.130675T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.254T=	ENSP00000434560.2:p.Val85=
ENST00000646564.2:c.478-12770T=	ENSP00000495806.2:n.478-12770T=
ENST00000155840.12:c.515T= MANE Select	ENSP00000155840.2:p.Val172=
ENST00000335475.6:c.134T=	ENSP00000334497.5:p.Val45=
ENST00000646564.1:c.124-12770T=	ENSP00000495806.1:n.124-12770T=
ENST00000155840.9:c.515T=	ENSP00000155840.2:p.Val172=
ENST00000335475.5:c.134T=	ENSP00000334497.5:p.Val45=
ENST00000496887.6:c.254T=	ENSP00000434560.1:p.Val85=
NM_000218.2:c.515T= , LRG_287t1:c.515T=	NP_000209.2:p.Val172=
NM_181798.1:c.134T= , LRG_287t2:c.134T=	NP_861463.1:p.Val45=
NM_000218.3:c.515T= MANE Select	NP_000209.2:p.Val172=