Canonical Allele Identifier: CA005355

Gene: KCNQ1

Linked Data

• ClinVar Variation Id: 52963
• ClinVar RCV Id: RCV000576927 ; RCV002223777
• dbSNP Id: rs397508078
• MyVariant Identifiers: chr11:g.2606538G>T (hg19) ; chr11:g.2585308G>T (hg38)
• PubMed: PMID:15840476

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2585308G>T , CM000673.2:g.2585308G>T	GRCh38
NC_000011.9:g.2606538G>T , CM000673.1:g.2606538G>T	GRCh37
NC_000011.8:g.2563114G>T	NCBI36
NG_008935.1:g.145318G>T , LRG_287:g.145318G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.771+1763G>T	ENSP00000434560.2:n.771+1763G>T
ENST00000646564.2:c.588+1763G>T	ENSP00000495806.2:n.588+1763G>T
ENST00000155840.12:c.1128+1G>T MANE Select	ENSP00000155840.2:n.1128+1G>T
ENST00000335475.6:c.747+1G>T	ENSP00000334497.5:n.747+1G>T
ENST00000646564.1:c.234+1763G>T	ENSP00000495806.1:n.234+1763G>T
ENST00000155840.9:c.1128+1G>T	ENSP00000155840.2:n.1128+1G>T
ENST00000335475.5:c.747+1G>T	ENSP00000334497.5:n.747+1G>T
NM_000218.2:c.1128+1G>T , LRG_287t1:c.1128+1G>T	NP_000209.2:n.1128+1G>T
NM_181798.1:c.747+1G>T , LRG_287t2:c.747+1G>T	NP_861463.1:n.747+1G>T
NM_000218.3:c.1128+1G>T MANE Select	NP_000209.2:n.1128+1G>T