Canonical Allele Identifier: CA472415605
Gene: KCNQ1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.2466343C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2445113C>G , CM000673.2:g.2445113C>G GRCh38
NC_000011.9:g.2466343C>G , CM000673.1:g.2466343C>G GRCh37
NC_000011.8:g.2422919C>G NCBI36
NG_008935.1:g.5123C>G , LRG_287:g.5123C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.24-270C>G ENSP00000434560.2:n.24-270C>G
ENST00000646564.2:c.15C>G ENSP00000495806.2:p.Ser5=
ENST00000155840.12:c.15C>G MANE Select ENSP00000155840.2:p.Ser5=
ENST00000155840.9:c.15C>G ENSP00000155840.2:p.Ser5=
ENST00000496887.6:c.24-270C>G ENSP00000434560.1:n.24-270C>G
NM_000218.2:c.15C>G , LRG_287t1:c.15C>G NP_000209.2:p.Ser5=
NM_000218.3:c.15C>G MANE Select NP_000209.2:p.Ser5=