Canonical Allele Identifier: CA1948233059
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2587584C= , CM000673.2:g.2587584C= GRCh38
NC_000011.9:g.2608814C= , CM000673.1:g.2608814C= GRCh37
NC_000011.8:g.2565390C= NCBI36
NG_008935.1:g.147594C= , LRG_287:g.147594C=

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.786C= ENSP00000434560.2:p.Cys262=
ENST00000646564.2:c.603C= ENSP00000495806.2:p.Cys201=
ENST00000155840.12:c.1143C= MANE Select ENSP00000155840.2:p.Cys381=
ENST00000335475.6:c.762C= ENSP00000334497.5:p.Cys254=
ENST00000646564.1:c.249C= ENSP00000495806.1:p.Cys83=
ENST00000155840.9:c.1143C= ENSP00000155840.2:p.Cys381=
ENST00000335475.5:c.762C= ENSP00000334497.5:p.Cys254=
NM_000218.2:c.1143C= , LRG_287t1:c.1143C= NP_000209.2:p.Cys381=
NM_181798.1:c.762C= , LRG_287t2:c.762C= NP_861463.1:p.Cys254=
NM_000218.3:c.1143C= MANE Select NP_000209.2:p.Cys381=