Canonical Allele Identifier: CA1948310322
Gene: KCNQ1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2769155C= , CM000673.2:g.2769155C= GRCh38
NC_000011.9:g.2790385C= , CM000673.1:g.2790385C= GRCh37
NC_000011.8:g.2746961C= NCBI36
NG_008935.1:g.329165C= , LRG_287:g.329165C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.1233+236C= ENSP00000434560.2:n.1233+236C=
ENST00000646564.2:c.1050+236C= ENSP00000495806.2:n.1050+236C=
ENST00000155840.12:c.1590+236C= MANE Select ENSP00000155840.2:n.1590+236C=
ENST00000335475.6:c.1209+236C= ENSP00000334497.5:n.1209+236C=
ENST00000646564.1:c.696+236C= ENSP00000495806.1:n.696+236C=
ENST00000155840.9:c.1590+236C= ENSP00000155840.2:n.1590+236C=
ENST00000335475.5:c.1209+236C= ENSP00000334497.5:n.1209+236C=
NM_000218.2:c.1590+236C= , LRG_287t1:c.1590+236C= NP_000209.2:n.1590+236C=
NM_181798.1:c.1209+236C= , LRG_287t2:c.1209+236C= NP_861463.1:n.1209+236C=
NM_000218.3:c.1590+236C= MANE Select NP_000209.2:n.1590+236C=
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