Canonical Allele Identifier: CA379116932
Gene: KCNQ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2445343G>C , CM000673.2:g.2445343G>C GRCh38
NC_000011.9:g.2466573G>C , CM000673.1:g.2466573G>C GRCh37
NC_000011.8:g.2423149G>C NCBI36
NG_008935.1:g.5353G>C , LRG_287:g.5353G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.24-40G>C ENSP00000434560.2:n.24-40G>C
ENST00000646564.2:c.245G>C ENSP00000495806.2:p.Arg82Pro
ENST00000155840.12:c.245G>C MANE Select ENSP00000155840.2:p.Arg82Pro
ENST00000155840.9:c.245G>C ENSP00000155840.2:p.Arg82Pro
ENST00000345015.4:n.22G>C
ENST00000496887.6:c.24-40G>C ENSP00000434560.1:n.24-40G>C
NM_000218.2:c.245G>C , LRG_287t1:c.245G>C NP_000209.2:p.Arg82Pro
NM_000218.3:c.245G>C MANE Select NP_000209.2:p.Arg82Pro