Canonical Allele Identifier: CA379133821

Gene: KCNQ1

Linked Data

• gnomAD v4: 11-2585267-A-G
• MyVariant Identifiers: chr11:g.2606497A>G (hg19) ; chr11:g.2585267A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2585267A>G , CM000673.2:g.2585267A>G	GRCh38
NC_000011.9:g.2606497A>G , CM000673.1:g.2606497A>G	GRCh37
NC_000011.8:g.2563073A>G	NCBI36
NG_008935.1:g.145277A>G , LRG_287:g.145277A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.771+1722A>G	ENSP00000434560.2:n.771+1722A>G
ENST00000646564.2:c.588+1722A>G	ENSP00000495806.2:n.588+1722A>G
ENST00000155840.12:c.1088A>G MANE Select	ENSP00000155840.2:p.His363Arg
ENST00000335475.6:c.707A>G	ENSP00000334497.5:p.His236Arg
ENST00000646564.1:c.234+1722A>G	ENSP00000495806.1:n.234+1722A>G
ENST00000155840.9:c.1088A>G	ENSP00000155840.2:p.His363Arg
ENST00000335475.5:c.707A>G	ENSP00000334497.5:p.His236Arg
NM_000218.2:c.1088A>G , LRG_287t1:c.1088A>G	NP_000209.2:p.His363Arg
NM_181798.1:c.707A>G , LRG_287t2:c.707A>G	NP_861463.1:p.His236Arg
NM_000218.3:c.1088A>G MANE Select	NP_000209.2:p.His363Arg