Canonical Allele Identifier: CA040589
Gene: KCNQ1 HGNC NCBI

Linked Data

dbSNP Id: rs765684768
gnomAD v2: 11-2594051-C-T
gnomAD v4: 11-2572821-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2572821C>T , CM000673.2:g.2572821C>T GRCh38
NC_000011.9:g.2594051C>T , CM000673.1:g.2594051C>T GRCh37
NC_000011.8:g.2550627C>T NCBI36
NG_008935.1:g.132831C>T , LRG_287:g.132831C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.520-25C>T ENSP00000434560.2:n.520-25C>T
ENST00000646564.2:c.478-10614C>T ENSP00000495806.2:n.478-10614C>T
ENST00000155840.12:c.781-25C>T MANE Select ENSP00000155840.2:n.781-25C>T
ENST00000335475.6:c.400-25C>T ENSP00000334497.5:n.400-25C>T
ENST00000646564.1:c.124-10614C>T ENSP00000495806.1:n.124-10614C>T
ENST00000155840.9:c.781-25C>T ENSP00000155840.2:n.781-25C>T
ENST00000335475.5:c.400-25C>T ENSP00000334497.5:n.400-25C>T
ENST00000496887.6:c.520-25C>T ENSP00000434560.1:n.520-25C>T
NM_000218.2:c.781-25C>T , LRG_287t1:c.781-25C>T NP_000209.2:n.781-25C>T
NM_181798.1:c.400-25C>T , LRG_287t2:c.400-25C>T NP_861463.1:n.400-25C>T
NM_000218.3:c.781-25C>T MANE Select NP_000209.2:n.781-25C>T