Canonical Allele Identifier: CA1948224796
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2583463A= , CM000673.2:g.2583463A= GRCh38
NC_000011.9:g.2604693A= , CM000673.1:g.2604693A= GRCh37
NC_000011.8:g.2561269A= NCBI36
NG_008935.1:g.143473A= , LRG_287:g.143473A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.689A= ENSP00000434560.2:p.Asp230=
ENST00000646564.2:c.506A= ENSP00000495806.2:p.Asp169=
ENST00000155840.12:c.950A= MANE Select ENSP00000155840.2:p.Asp317=
ENST00000335475.6:c.569A= ENSP00000334497.5:p.Asp190=
ENST00000646564.1:c.152A= ENSP00000495806.1:p.Asp51=
ENST00000155840.9:c.950A= ENSP00000155840.2:p.Asp317=
ENST00000335475.5:c.569A= ENSP00000334497.5:p.Asp190=
NM_000218.2:c.950A= , LRG_287t1:c.950A= NP_000209.2:p.Asp317=
NM_181798.1:c.569A= , LRG_287t2:c.569A= NP_861463.1:p.Asp190=
NM_000218.3:c.950A= MANE Select NP_000209.2:p.Asp317=