Canonical Allele Identifier: CA004932
Gene: KCNQ1 HGNC NCBI

Linked Data

ClinVar Variation Id: 52934
ClinVar RCV Id: RCV000057531
dbSNP Id: rs199472761

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2583541C>G , CM000673.2:g.2583541C>G GRCh38
NC_000011.9:g.2604771C>G , CM000673.1:g.2604771C>G GRCh37
NC_000011.8:g.2561347C>G NCBI36
NG_008935.1:g.143551C>G , LRG_287:g.143551C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.767C>G ENSP00000434560.2:p.Pro256Arg
ENST00000646564.2:c.584C>G ENSP00000495806.2:p.Pro195Arg
ENST00000155840.12:c.1028C>G MANE Select ENSP00000155840.2:p.Pro343Arg
ENST00000335475.6:c.647C>G ENSP00000334497.5:p.Pro216Arg
ENST00000646564.1:c.230C>G ENSP00000495806.1:p.Pro77Arg
ENST00000155840.9:c.1028C>G ENSP00000155840.2:p.Pro343Arg
ENST00000335475.5:c.647C>G ENSP00000334497.5:p.Pro216Arg
NM_000218.2:c.1028C>G , LRG_287t1:c.1028C>G NP_000209.2:p.Pro343Arg
NM_181798.1:c.647C>G , LRG_287t2:c.647C>G NP_861463.1:p.Pro216Arg
NM_000218.3:c.1028C>G MANE Select NP_000209.2:p.Pro343Arg