Canonical Allele Identifier: CA2612007045
Gene: KCNQ1 HGNC NCBI
KCNQ1OT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2662027_2662032dup , CM000673.2:g.2662027_2662032dup GRCh38
NC_000011.9:g.2683257_2683262dup , CM000673.1:g.2683257_2683262dup GRCh37
NC_000011.8:g.2639833_2639838dup NCBI36
NG_008935.1:g.222037_222042dup , LRG_287:g.222037_222042dup
NG_016178.2:g.42967_42972dup

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.1103_1108dup (KCNQ1) ENSP00000434560.2:p.Asp369_Leu370insGlnAs...
ENST00000646564.2:c.920_925dup (KCNQ1) ENSP00000495806.2:p.Asp308_Leu309insGlnAs...
ENST00000155840.12:c.1460_1465dup (KCNQ1) MANE Select ENSP00000155840.2:p.Asp488_Leu489insGlnAs...
ENST00000335475.6:c.1079_1084dup (KCNQ1) ENSP00000334497.5:p.Asp361_Leu362insGlnAs...
ENST00000646564.1:c.566_571dup (KCNQ1) ENSP00000495806.1:p.Asp190_Leu191insGlnAs...
ENST00000155840.9:c.1460_1465dup (KCNQ1) ENSP00000155840.2:p.Asp488_Leu489insGlnAs...
ENST00000335475.5:c.1079_1084dup (KCNQ1) ENSP00000334497.5:p.Asp361_Leu362insGlnAs...
NM_000218.2:c.1460_1465dup , LRG_287t1:c.1460_1465dup (KCNQ1) NP_000209.2:p.Asp488_Leu489insGlnAsp
NM_181798.1:c.1079_1084dup , LRG_287t2:c.1079_1084dup (KCNQ1) NP_861463.1:p.Asp361_Leu362insGlnAsp
NR_002728.3:n.37967_37972dup (KCNQ1OT1)
NM_000218.3:c.1460_1465dup (KCNQ1) MANE Select NP_000209.2:p.Asp488_Leu489insGlnAsp