Canonical Allele Identifier: CA040953
Gene: KCNQ1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2196415
ClinVar RCV Id: RCV002633652
dbSNP Id: rs776982883
gnomAD v2: 11-2594150-G-A
gnomAD v4: 11-2572920-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2572920G>A , CM000673.2:g.2572920G>A GRCh38
NC_000011.9:g.2594150G>A , CM000673.1:g.2594150G>A GRCh37
NC_000011.8:g.2550726G>A NCBI36
NG_008935.1:g.132930G>A , LRG_287:g.132930G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.594G>A ENSP00000434560.2:p.Lys198=
ENST00000646564.2:c.478-10515G>A ENSP00000495806.2:n.478-10515G>A
ENST00000155840.12:c.855G>A MANE Select ENSP00000155840.2:p.Lys285=
ENST00000335475.6:c.474G>A ENSP00000334497.5:p.Lys158=
ENST00000646564.1:c.124-10515G>A ENSP00000495806.1:n.124-10515G>A
ENST00000155840.9:c.855G>A ENSP00000155840.2:p.Lys285=
ENST00000335475.5:c.474G>A ENSP00000334497.5:p.Lys158=
NM_000218.2:c.855G>A , LRG_287t1:c.855G>A NP_000209.2:p.Lys285=
NM_181798.1:c.474G>A , LRG_287t2:c.474G>A NP_861463.1:p.Lys158=
NM_000218.3:c.855G>A MANE Select NP_000209.2:p.Lys285=