Canonical Allele Identifier: CA379131279
Gene: KCNQ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2572855A>G , CM000673.2:g.2572855A>G GRCh38
NC_000011.9:g.2594085A>G , CM000673.1:g.2594085A>G GRCh37
NC_000011.8:g.2550661A>G NCBI36
NG_008935.1:g.132865A>G , LRG_287:g.132865A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.529A>G ENSP00000434560.2:p.Thr177Ala
ENST00000646564.2:c.478-10580A>G ENSP00000495806.2:n.478-10580A>G
ENST00000155840.12:c.790A>G MANE Select ENSP00000155840.2:p.Thr264Ala
ENST00000335475.6:c.409A>G ENSP00000334497.5:p.Thr137Ala
ENST00000646564.1:c.124-10580A>G ENSP00000495806.1:n.124-10580A>G
ENST00000155840.9:c.790A>G ENSP00000155840.2:p.Thr264Ala
ENST00000335475.5:c.409A>G ENSP00000334497.5:p.Thr137Ala
ENST00000496887.6:c.529A>G ENSP00000434560.1:p.Thr177Ala
NM_000218.2:c.790A>G , LRG_287t1:c.790A>G NP_000209.2:p.Thr264Ala
NM_181798.1:c.409A>G , LRG_287t2:c.409A>G NP_861463.1:p.Thr137Ala
NM_000218.3:c.790A>G MANE Select NP_000209.2:p.Thr264Ala