Canonical Allele Identifier: CA1948171479
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2463531C= , CM000673.2:g.2463531C= GRCh38
NC_000011.9:g.2484761C= , CM000673.1:g.2484761C= GRCh37
NC_000011.8:g.2441337C= NCBI36
NG_008935.1:g.23541C= , LRG_287:g.23541C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000380776.5:n.91+1554C=
ENST00000496887.7:c.125+18047C= ENSP00000434560.2:n.125+18047C=
ENST00000646564.2:c.386+18047C= ENSP00000495806.2:n.386+18047C=
ENST00000155840.12:c.386+18047C= MANE Select ENSP00000155840.2:n.386+18047C=
ENST00000335475.6:c.5+1817C= ENSP00000334497.5:n.5+1817C=
ENST00000646564.1:c.32+18047C= ENSP00000495806.1:n.32+18047C=
ENST00000155840.9:c.386+18047C= ENSP00000155840.2:n.386+18047C=
ENST00000335475.5:c.5+1817C= ENSP00000334497.5:n.5+1817C=
ENST00000345015.4:n.163+18047C=
ENST00000380776.4:c.84+1554C= ENSP00000370153.4:n.84+1554C=
ENST00000496887.6:c.125+18047C= ENSP00000434560.1:n.125+18047C=
NM_000218.2:c.386+18047C= , LRG_287t1:c.386+18047C= NP_000209.2:n.386+18047C=
NM_181798.1:c.5+1817C= , LRG_287t2:c.5+1817C= NP_861463.1:n.5+1817C=
NM_000218.3:c.386+18047C= MANE Select NP_000209.2:n.386+18047C=