Canonical Allele Identifier: CA216327074

Gene: KCNQ1

Linked Data

• dbSNP Id: rs1012311639
• gnomAD v2: 11-2604643-A-G
• gnomAD v4: 11-2583413-A-G
• MyVariant Identifiers: chr11:g.2604643A>G (hg19) ; chr11:g.2583413A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2583413A>G , CM000673.2:g.2583413A>G	GRCh38
NC_000011.9:g.2604643A>G , CM000673.1:g.2604643A>G	GRCh37
NC_000011.8:g.2561219A>G	NCBI36
NG_008935.1:g.143423A>G , LRG_287:g.143423A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.661-22A>G	ENSP00000434560.2:n.661-22A>G
ENST00000646564.2:c.478-22A>G	ENSP00000495806.2:n.478-22A>G
ENST00000155840.12:c.922-22A>G MANE Select	ENSP00000155840.2:n.922-22A>G
ENST00000335475.6:c.541-22A>G	ENSP00000334497.5:n.541-22A>G
ENST00000646564.1:c.124-22A>G	ENSP00000495806.1:n.124-22A>G
ENST00000155840.9:c.922-22A>G	ENSP00000155840.2:n.922-22A>G
ENST00000335475.5:c.541-22A>G	ENSP00000334497.5:n.541-22A>G
NM_000218.2:c.922-22A>G , LRG_287t1:c.922-22A>G	NP_000209.2:n.922-22A>G
NM_181798.1:c.541-22A>G , LRG_287t2:c.541-22A>G	NP_861463.1:n.541-22A>G
NM_000218.3:c.922-22A>G MANE Select	NP_000209.2:n.922-22A>G