Canonical Allele Identifier: CA379131542
Gene: KCNQ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2572920G>C , CM000673.2:g.2572920G>C GRCh38
NC_000011.9:g.2594150G>C , CM000673.1:g.2594150G>C GRCh37
NC_000011.8:g.2550726G>C NCBI36
NG_008935.1:g.132930G>C , LRG_287:g.132930G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.594G>C ENSP00000434560.2:p.Lys198Asn
ENST00000646564.2:c.478-10515G>C ENSP00000495806.2:n.478-10515G>C
ENST00000155840.12:c.855G>C MANE Select ENSP00000155840.2:p.Lys285Asn
ENST00000335475.6:c.474G>C ENSP00000334497.5:p.Lys158Asn
ENST00000646564.1:c.124-10515G>C ENSP00000495806.1:n.124-10515G>C
ENST00000155840.9:c.855G>C ENSP00000155840.2:p.Lys285Asn
ENST00000335475.5:c.474G>C ENSP00000334497.5:p.Lys158Asn
NM_000218.2:c.855G>C , LRG_287t1:c.855G>C NP_000209.2:p.Lys285Asn
NM_181798.1:c.474G>C , LRG_287t2:c.474G>C NP_861463.1:p.Lys158Asn
NM_000218.3:c.855G>C MANE Select NP_000209.2:p.Lys285Asn