Canonical Allele Identifier: CA379138947
Gene: KCNQ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2768872A>G , CM000673.2:g.2768872A>G GRCh38
NC_000011.9:g.2790102A>G , CM000673.1:g.2790102A>G GRCh37
NC_000011.8:g.2746678A>G NCBI36
NG_008935.1:g.328882A>G , LRG_287:g.328882A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.1186A>G ENSP00000434560.2:p.Lys396Glu
ENST00000646564.2:c.1003A>G ENSP00000495806.2:p.Lys335Glu
ENST00000155840.12:c.1543A>G MANE Select ENSP00000155840.2:p.Lys515Glu
ENST00000335475.6:c.1162A>G ENSP00000334497.5:p.Lys388Glu
ENST00000646564.1:c.649A>G ENSP00000495806.1:p.Lys217Glu
ENST00000155840.9:c.1543A>G ENSP00000155840.2:p.Lys515Glu
ENST00000335475.5:c.1162A>G ENSP00000334497.5:p.Lys388Glu
NM_000218.2:c.1543A>G , LRG_287t1:c.1543A>G NP_000209.2:p.Lys515Glu
NM_181798.1:c.1162A>G , LRG_287t2:c.1162A>G NP_861463.1:p.Lys388Glu
NM_000218.3:c.1543A>G MANE Select NP_000209.2:p.Lys515Glu