Canonical Allele Identifier: CA1948224839
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2583470G= , CM000673.2:g.2583470G= GRCh38
NC_000011.9:g.2604700G= , CM000673.1:g.2604700G= GRCh37
NC_000011.8:g.2561276G= NCBI36
NG_008935.1:g.143480G= , LRG_287:g.143480G=

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.696G= ENSP00000434560.2:p.Val232=
ENST00000646564.2:c.513G= ENSP00000495806.2:p.Val171=
ENST00000155840.12:c.957G= MANE Select ENSP00000155840.2:p.Val319=
ENST00000335475.6:c.576G= ENSP00000334497.5:p.Val192=
ENST00000646564.1:c.159G= ENSP00000495806.1:p.Val53=
ENST00000155840.9:c.957G= ENSP00000155840.2:p.Val319=
ENST00000335475.5:c.576G= ENSP00000334497.5:p.Val192=
NM_000218.2:c.957G= , LRG_287t1:c.957G= NP_000209.2:p.Val319=
NM_181798.1:c.576G= , LRG_287t2:c.576G= NP_861463.1:p.Val192=
NM_000218.3:c.957G= MANE Select NP_000209.2:p.Val319=