Canonical Allele Identifier: CA472415599
Gene: KCNQ1 HGNC NCBI

Linked Data

gnomAD v4: 11-2445107-G-T
MyVariant Identifiers: chr11:g.2466337G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2445107G>T , CM000673.2:g.2445107G>T GRCh38
NC_000011.9:g.2466337G>T , CM000673.1:g.2466337G>T GRCh37
NC_000011.8:g.2422913G>T NCBI36
NG_008935.1:g.5117G>T , LRG_287:g.5117G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.24-276G>T ENSP00000434560.2:n.24-276G>T
ENST00000646564.2:c.9G>T ENSP00000495806.2:p.Ala3=
ENST00000155840.12:c.9G>T MANE Select ENSP00000155840.2:p.Ala3=
ENST00000155840.9:c.9G>T ENSP00000155840.2:p.Ala3=
ENST00000496887.6:c.24-276G>T ENSP00000434560.1:n.24-276G>T
NM_000218.2:c.9G>T , LRG_287t1:c.9G>T NP_000209.2:p.Ala3=
NM_000218.3:c.9G>T MANE Select NP_000209.2:p.Ala3=