Canonical Allele Identifier: CA934460159
Gene: KCNQ1 HGNC NCBI

Linked Data

dbSNP Id: rs1848340422

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2571920del , CM000673.2:g.2571920del GRCh38
NC_000011.9:g.2593150del , CM000673.1:g.2593150del GRCh37
NC_000011.8:g.2549726del NCBI36
NG_008935.1:g.131930del , LRG_287:g.131930del

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.423-93del ENSP00000434560.2:n.423-93del
ENST00000646564.2:c.478-11515del ENSP00000495806.2:n.478-11515del
ENST00000155840.12:c.684-93del MANE Select ENSP00000155840.2:n.684-93del
ENST00000335475.6:c.303-93del ENSP00000334497.5:n.303-93del
ENST00000646564.1:c.124-11515del ENSP00000495806.1:n.124-11515del
ENST00000155840.9:c.684-93del ENSP00000155840.2:n.684-93del
ENST00000335475.5:c.303-93del ENSP00000334497.5:n.303-93del
ENST00000496887.6:c.423-93del ENSP00000434560.1:n.423-93del
NM_000218.2:c.684-93del , LRG_287t1:c.684-93del NP_000209.2:n.684-93del
NM_181798.1:c.303-93del , LRG_287t2:c.303-93del NP_861463.1:n.303-93del
NM_000218.3:c.684-93del MANE Select NP_000209.2:n.684-93del