Canonical Allele Identifier: CA379115688
Gene: KCNQ1 HGNC NCBI

Linked Data

gnomAD v4: 11-2445105-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2445105G>A , CM000673.2:g.2445105G>A GRCh38
NC_000011.9:g.2466335G>A , CM000673.1:g.2466335G>A GRCh37
NC_000011.8:g.2422911G>A NCBI36
NG_008935.1:g.5115G>A , LRG_287:g.5115G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.24-278G>A ENSP00000434560.2:n.24-278G>A
ENST00000646564.2:c.7G>A ENSP00000495806.2:p.Ala3Thr
ENST00000155840.12:c.7G>A MANE Select ENSP00000155840.2:p.Ala3Thr
ENST00000155840.9:c.7G>A ENSP00000155840.2:p.Ala3Thr
ENST00000496887.6:c.24-278G>A ENSP00000434560.1:n.24-278G>A
NM_000218.2:c.7G>A , LRG_287t1:c.7G>A NP_000209.2:p.Ala3Thr
NM_000218.3:c.7G>A MANE Select NP_000209.2:p.Ala3Thr