Canonical Allele Identifier: CA597109388
Gene: KCNQ1 HGNC NCBI

Linked Data

ClinVar Variation Id: 527102
dbSNP Id: rs1212611138
gnomAD v2: 11-2593238-C-T
gnomAD v3: 11-2572008-C-T
gnomAD v4: 11-2572008-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2572008C>T , CM000673.2:g.2572008C>T GRCh38
NC_000011.9:g.2593238C>T , CM000673.1:g.2593238C>T GRCh37
NC_000011.8:g.2549814C>T NCBI36
NG_008935.1:g.132018C>T , LRG_287:g.132018C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.423-5C>T ENSP00000434560.2:n.423-5C>T
ENST00000646564.2:c.478-11427C>T ENSP00000495806.2:n.478-11427C>T
ENST00000155840.12:c.684-5C>T MANE Select ENSP00000155840.2:n.684-5C>T
ENST00000335475.6:c.303-5C>T ENSP00000334497.5:n.303-5C>T
ENST00000646564.1:c.124-11427C>T ENSP00000495806.1:n.124-11427C>T
ENST00000155840.9:c.684-5C>T ENSP00000155840.2:n.684-5C>T
ENST00000335475.5:c.303-5C>T ENSP00000334497.5:n.303-5C>T
ENST00000496887.6:c.423-5C>T ENSP00000434560.1:n.423-5C>T
NM_000218.2:c.684-5C>T , LRG_287t1:c.684-5C>T NP_000209.2:n.684-5C>T
NM_181798.1:c.303-5C>T , LRG_287t2:c.303-5C>T NP_861463.1:n.303-5C>T
NM_000218.3:c.684-5C>T MANE Select NP_000209.2:n.684-5C>T