Canonical Allele Identifier: CA2723229569
Gene: KCNQ1 HGNC NCBI

Linked Data

dbSNP Id: rs2133750160

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2583200del , CM000673.2:g.2583200del GRCh38
NC_000011.9:g.2604430del , CM000673.1:g.2604430del GRCh37
NC_000011.8:g.2561006del NCBI36
NG_008935.1:g.143210del , LRG_287:g.143210del

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.661-235del ENSP00000434560.2:n.661-235del
ENST00000646564.2:c.478-235del ENSP00000495806.2:n.478-235del
ENST00000155840.12:c.922-235del MANE Select ENSP00000155840.2:n.922-235del
ENST00000335475.6:c.541-235del ENSP00000334497.5:n.541-235del
ENST00000646564.1:c.124-235del ENSP00000495806.1:n.124-235del
ENST00000155840.9:c.922-235del ENSP00000155840.2:n.922-235del
ENST00000335475.5:c.541-235del ENSP00000334497.5:n.541-235del
NM_000218.2:c.922-235del , LRG_287t1:c.922-235del NP_000209.2:n.922-235del
NM_181798.1:c.541-235del , LRG_287t2:c.541-235del NP_861463.1:n.541-235del
NM_000218.3:c.922-235del MANE Select NP_000209.2:n.922-235del