Canonical Allele Identifier: CA216319196
Gene: KCNQ1 HGNC NCBI

Linked Data

dbSNP Id: rs921981042
gnomAD v2: 11-2549074-A-G
gnomAD v3: 11-2527844-A-G
gnomAD v4: 11-2527844-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2527844A>G , CM000673.2:g.2527844A>G GRCh38
NC_000011.9:g.2549074A>G , CM000673.1:g.2549074A>G GRCh37
NC_000011.8:g.2505650A>G NCBI36
NG_008935.1:g.87854A>G , LRG_287:g.87854A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000380776.5:n.184-84A>G
ENST00000496887.7:c.126-84A>G ENSP00000434560.2:n.126-84A>G
ENST00000646564.2:c.387-84A>G ENSP00000495806.2:n.387-84A>G
ENST00000155840.12:c.387-84A>G MANE Select ENSP00000155840.2:n.387-84A>G
ENST00000335475.6:c.6-84A>G ENSP00000334497.5:n.6-84A>G
ENST00000646564.1:c.33-84A>G ENSP00000495806.1:n.33-84A>G
ENST00000155840.9:c.387-84A>G ENSP00000155840.2:n.387-84A>G
ENST00000335475.5:c.6-84A>G ENSP00000334497.5:n.6-84A>G
ENST00000345015.4:n.256-84A>G
ENST00000380776.4:c.177-84A>G ENSP00000370153.4:n.177-84A>G
ENST00000496887.6:c.126-84A>G ENSP00000434560.1:n.126-84A>G
NM_000218.2:c.387-84A>G , LRG_287t1:c.387-84A>G NP_000209.2:n.387-84A>G
NM_181798.1:c.6-84A>G , LRG_287t2:c.6-84A>G NP_861463.1:n.6-84A>G
NM_000218.3:c.387-84A>G MANE Select NP_000209.2:n.387-84A>G