Canonical Allele Identifier: CA2611999653
Gene: KCNQ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2445062del , CM000673.2:g.2445062del GRCh38
NC_000011.9:g.2466292del , CM000673.1:g.2466292del GRCh37
NC_000011.8:g.2422868del NCBI36
NG_008935.1:g.5072del , LRG_287:g.5072del

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.24-321del ENSP00000434560.2:n.24-321del
ENST00000646564.2:c.-37del ENSP00000495806.2:n.-37del
ENST00000155840.12:c.-37del MANE Select ENSP00000155840.2:n.-37del
ENST00000155840.9:c.-37del ENSP00000155840.2:n.-37del
ENST00000496887.6:c.24-321del ENSP00000434560.1:n.24-321del
NM_000218.2:c.-37del , LRG_287t1:c.-37del NP_000209.2:n.-37del
NM_000218.3:c.-37del MANE Select NP_000209.2:n.-37del