Canonical Allele Identifier: CA1948224341
Gene: KCNQ1 HGNC NCBI

Linked Data

dbSNP Id: rs1848531707

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2583295del , CM000673.2:g.2583295del GRCh38
NC_000011.9:g.2604525del , CM000673.1:g.2604525del GRCh37
NC_000011.8:g.2561101del NCBI36
NG_008935.1:g.143305del , LRG_287:g.143305del

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.661-140del ENSP00000434560.2:n.661-140del
ENST00000646564.2:c.478-140del ENSP00000495806.2:n.478-140del
ENST00000155840.12:c.922-140del MANE Select ENSP00000155840.2:n.922-140del
ENST00000335475.6:c.541-140del ENSP00000334497.5:n.541-140del
ENST00000646564.1:c.124-140del ENSP00000495806.1:n.124-140del
ENST00000155840.9:c.922-140del ENSP00000155840.2:n.922-140del
ENST00000335475.5:c.541-140del ENSP00000334497.5:n.541-140del
NM_000218.2:c.922-140del , LRG_287t1:c.922-140del NP_000209.2:n.922-140del
NM_181798.1:c.541-140del , LRG_287t2:c.541-140del NP_861463.1:n.541-140del
NM_000218.3:c.922-140del MANE Select NP_000209.2:n.922-140del