Canonical Allele Identifier: CA008832
Gene: KCNQ1 HGNC NCBI

Linked Data

ClinVar Variation Id: 53143
ClinVar RCV Id: RCV000057819
dbSNP Id: rs104894255

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2583459G>C , CM000673.2:g.2583459G>C GRCh38
NC_000011.9:g.2604689G>C , CM000673.1:g.2604689G>C GRCh37
NC_000011.8:g.2561265G>C NCBI36
NG_008935.1:g.143469G>C , LRG_287:g.143469G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.685G>C ENSP00000434560.2:p.Gly229Arg
ENST00000646564.2:c.502G>C ENSP00000495806.2:p.Gly168Arg
ENST00000155840.12:c.946G>C MANE Select ENSP00000155840.2:p.Gly316Arg
ENST00000335475.6:c.565G>C ENSP00000334497.5:p.Gly189Arg
ENST00000646564.1:c.148G>C ENSP00000495806.1:p.Gly50Arg
ENST00000155840.9:c.946G>C ENSP00000155840.2:p.Gly316Arg
ENST00000335475.5:c.565G>C ENSP00000334497.5:p.Gly189Arg
NM_000218.2:c.946G>C , LRG_287t1:c.946G>C NP_000209.2:p.Gly316Arg
NM_181798.1:c.565G>C , LRG_287t2:c.565G>C NP_861463.1:p.Gly189Arg
NM_000218.3:c.946G>C MANE Select NP_000209.2:p.Gly316Arg