Canonical Allele Identifier: CA472038508

Gene: KCNQ1

Linked Data

• ClinVar Variation Id: 2877363
• ClinVar RCV Id: RCV003648687
• dbSNP Id: rs199473663
• gnomAD v4: 11-2585280-G-A
• MyVariant Identifiers: chr11:g.2606510G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2585280G>A , CM000673.2:g.2585280G>A	GRCh38
NC_000011.9:g.2606510G>A , CM000673.1:g.2606510G>A	GRCh37
NC_000011.8:g.2563086G>A	NCBI36
NG_008935.1:g.145290G>A , LRG_287:g.145290G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.771+1735G>A	ENSP00000434560.2:n.771+1735G>A
ENST00000646564.2:c.588+1735G>A	ENSP00000495806.2:n.588+1735G>A
ENST00000155840.12:c.1101G>A MANE Select	ENSP00000155840.2:p.Gln367=
ENST00000335475.6:c.720G>A	ENSP00000334497.5:p.Gln240=
ENST00000646564.1:c.234+1735G>A	ENSP00000495806.1:n.234+1735G>A
ENST00000155840.9:c.1101G>A	ENSP00000155840.2:p.Gln367=
ENST00000335475.5:c.720G>A	ENSP00000334497.5:p.Gln240=
NM_000218.2:c.1101G>A , LRG_287t1:c.1101G>A	NP_000209.2:p.Gln367=
NM_181798.1:c.720G>A , LRG_287t2:c.720G>A	NP_861463.1:p.Gln240=
NM_000218.3:c.1101G>A MANE Select	NP_000209.2:p.Gln367=