Canonical Allele Identifier: CA026830

Gene: KCNQ1

Linked Data

• ClinVar Variation Id: 1614470
• ClinVar RCV Id: RCV002075996
• dbSNP Id: rs760839693
• ExAC: 11:2604782 G / A
• gnomAD v2: 11-2604782-G-A
• gnomAD v4: 11-2583552-G-A
• MyVariant Identifiers: chr11:g.2604782G>A (hg19) ; chr11:g.2583552G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2583552G>A , CM000673.2:g.2583552G>A	GRCh38
NC_000011.9:g.2604782G>A , CM000673.1:g.2604782G>A	GRCh37
NC_000011.8:g.2561358G>A	NCBI36
NG_008935.1:g.143562G>A , LRG_287:g.143562G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.771+7G>A	ENSP00000434560.2:n.771+7G>A
ENST00000646564.2:c.588+7G>A	ENSP00000495806.2:n.588+7G>A
ENST00000155840.12:c.1032+7G>A MANE Select	ENSP00000155840.2:n.1032+7G>A
ENST00000335475.6:c.651+7G>A	ENSP00000334497.5:n.651+7G>A
ENST00000646564.1:c.234+7G>A	ENSP00000495806.1:n.234+7G>A
ENST00000155840.9:c.1032+7G>A	ENSP00000155840.2:n.1032+7G>A
ENST00000335475.5:c.651+7G>A	ENSP00000334497.5:n.651+7G>A
NM_000218.2:c.1032+7G>A , LRG_287t1:c.1032+7G>A	NP_000209.2:n.1032+7G>A
NM_181798.1:c.651+7G>A , LRG_287t2:c.651+7G>A	NP_861463.1:n.651+7G>A
NM_000218.3:c.1032+7G>A MANE Select	NP_000209.2:n.1032+7G>A