Canonical Allele Identifier: CA379132990
Gene: KCNQ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2583465A>G , CM000673.2:g.2583465A>G GRCh38
NC_000011.9:g.2604695A>G , CM000673.1:g.2604695A>G GRCh37
NC_000011.8:g.2561271A>G NCBI36
NG_008935.1:g.143475A>G , LRG_287:g.143475A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.691A>G ENSP00000434560.2:p.Lys231Glu
ENST00000646564.2:c.508A>G ENSP00000495806.2:p.Lys170Glu
ENST00000155840.12:c.952A>G MANE Select ENSP00000155840.2:p.Lys318Glu
ENST00000335475.6:c.571A>G ENSP00000334497.5:p.Lys191Glu
ENST00000646564.1:c.154A>G ENSP00000495806.1:p.Lys52Glu
ENST00000155840.9:c.952A>G ENSP00000155840.2:p.Lys318Glu
ENST00000335475.5:c.571A>G ENSP00000334497.5:p.Lys191Glu
NM_000218.2:c.952A>G , LRG_287t1:c.952A>G NP_000209.2:p.Lys318Glu
NM_181798.1:c.571A>G , LRG_287t2:c.571A>G NP_861463.1:p.Lys191Glu
NM_000218.3:c.952A>G MANE Select NP_000209.2:p.Lys318Glu