Canonical Allele Identifier: CA379131576

Gene: KCNQ1

Linked Data

• ClinVar Variation Id: 2800725
• ClinVar RCV Id: RCV003647488
• MyVariant Identifiers: chr11:g.2594164A>G (hg19) ; chr11:g.2572934A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2572934A>G , CM000673.2:g.2572934A>G	GRCh38
NC_000011.9:g.2594164A>G , CM000673.1:g.2594164A>G	GRCh37
NC_000011.8:g.2550740A>G	NCBI36
NG_008935.1:g.132944A>G , LRG_287:g.132944A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.608A>G	ENSP00000434560.2:p.Glu203Gly
ENST00000646564.2:c.478-10501A>G	ENSP00000495806.2:n.478-10501A>G
ENST00000155840.12:c.869A>G MANE Select	ENSP00000155840.2:p.Glu290Gly
ENST00000335475.6:c.488A>G	ENSP00000334497.5:p.Glu163Gly
ENST00000646564.1:c.124-10501A>G	ENSP00000495806.1:n.124-10501A>G
ENST00000155840.9:c.869A>G	ENSP00000155840.2:p.Glu290Gly
ENST00000335475.5:c.488A>G	ENSP00000334497.5:p.Glu163Gly
NM_000218.2:c.869A>G , LRG_287t1:c.869A>G	NP_000209.2:p.Glu290Gly
NM_181798.1:c.488A>G , LRG_287t2:c.488A>G	NP_861463.1:p.Glu163Gly
NM_000218.3:c.869A>G MANE Select	NP_000209.2:p.Glu290Gly