Canonical Allele Identifier: CA277170
Gene: KCNQ1 HGNC NCBI

Linked Data

ClinVar Variation Id: 200915
dbSNP Id: rs397508109

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2445462dup , CM000673.2:g.2445462dup GRCh38
NC_000011.9:g.2466692dup , CM000673.1:g.2466692dup GRCh37
NC_000011.8:g.2423268dup NCBI36
NG_008935.1:g.5472dup , LRG_287:g.5472dup

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.103dup ENSP00000434560.2:p.Cys35LeufsTer?
ENST00000646564.2:c.364dup ENSP00000495806.2:p.Cys122LeufsTer?
ENST00000155840.12:c.364dup MANE Select ENSP00000155840.2:p.Cys122LeufsTer?
ENST00000646564.1:c.10dup ENSP00000495806.1:p.Cys4LeufsTer?
ENST00000155840.9:c.364dup ENSP00000155840.2:p.Cys122LeufsTer?
ENST00000345015.4:n.141dup
ENST00000496887.6:c.103dup ENSP00000434560.1:p.Cys35LeufsTer?
NM_000218.2:c.364dup , LRG_287t1:c.364dup NP_000209.2:p.Cys122LeufsTer?
NM_000218.3:c.364dup MANE Select NP_000209.2:p.Cys122LeufsTer?