Canonical Allele Identifier: CA379134660
Gene: KCNQ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2587582T>C , CM000673.2:g.2587582T>C GRCh38
NC_000011.9:g.2608812T>C , CM000673.1:g.2608812T>C GRCh37
NC_000011.8:g.2565388T>C NCBI36
NG_008935.1:g.147592T>C , LRG_287:g.147592T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.784T>C ENSP00000434560.2:p.Cys262Arg
ENST00000646564.2:c.601T>C ENSP00000495806.2:p.Cys201Arg
ENST00000155840.12:c.1141T>C MANE Select ENSP00000155840.2:p.Cys381Arg
ENST00000335475.6:c.760T>C ENSP00000334497.5:p.Cys254Arg
ENST00000646564.1:c.247T>C ENSP00000495806.1:p.Cys83Arg
ENST00000155840.9:c.1141T>C ENSP00000155840.2:p.Cys381Arg
ENST00000335475.5:c.760T>C ENSP00000334497.5:p.Cys254Arg
NM_000218.2:c.1141T>C , LRG_287t1:c.1141T>C NP_000209.2:p.Cys381Arg
NM_181798.1:c.760T>C , LRG_287t2:c.760T>C NP_861463.1:p.Cys254Arg
NM_000218.3:c.1141T>C MANE Select NP_000209.2:p.Cys381Arg