Canonical Allele Identifier: CA379131530
Gene: KCNQ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2572918A>G , CM000673.2:g.2572918A>G GRCh38
NC_000011.9:g.2594148A>G , CM000673.1:g.2594148A>G GRCh37
NC_000011.8:g.2550724A>G NCBI36
NG_008935.1:g.132928A>G , LRG_287:g.132928A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.592A>G ENSP00000434560.2:p.Lys198Glu
ENST00000646564.2:c.478-10517A>G ENSP00000495806.2:n.478-10517A>G
ENST00000155840.12:c.853A>G MANE Select ENSP00000155840.2:p.Lys285Glu
ENST00000335475.6:c.472A>G ENSP00000334497.5:p.Lys158Glu
ENST00000646564.1:c.124-10517A>G ENSP00000495806.1:n.124-10517A>G
ENST00000155840.9:c.853A>G ENSP00000155840.2:p.Lys285Glu
ENST00000335475.5:c.472A>G ENSP00000334497.5:p.Lys158Glu
NM_000218.2:c.853A>G , LRG_287t1:c.853A>G NP_000209.2:p.Lys285Glu
NM_181798.1:c.472A>G , LRG_287t2:c.472A>G NP_861463.1:p.Lys158Glu
NM_000218.3:c.853A>G MANE Select NP_000209.2:p.Lys285Glu