Canonical Allele Identifier: CA1948224499
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2583415C= , CM000673.2:g.2583415C= GRCh38
NC_000011.9:g.2604645C= , CM000673.1:g.2604645C= GRCh37
NC_000011.8:g.2561221C= NCBI36
NG_008935.1:g.143425C= , LRG_287:g.143425C=

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.661-20C= ENSP00000434560.2:n.661-20C=
ENST00000646564.2:c.478-20C= ENSP00000495806.2:n.478-20C=
ENST00000155840.12:c.922-20C= MANE Select ENSP00000155840.2:n.922-20C=
ENST00000335475.6:c.541-20C= ENSP00000334497.5:n.541-20C=
ENST00000646564.1:c.124-20C= ENSP00000495806.1:n.124-20C=
ENST00000155840.9:c.922-20C= ENSP00000155840.2:n.922-20C=
ENST00000335475.5:c.541-20C= ENSP00000334497.5:n.541-20C=
NM_000218.2:c.922-20C= , LRG_287t1:c.922-20C= NP_000209.2:n.922-20C=
NM_181798.1:c.541-20C= , LRG_287t2:c.541-20C= NP_861463.1:n.541-20C=
NM_000218.3:c.922-20C= MANE Select NP_000209.2:n.922-20C=