Canonical Allele Identifier: CA2723227889

Gene: KCNQ1

Linked Data

• dbSNP Id: rs2133729914

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2571841_2571842del , CM000673.2:g.2571841_2571842del	GRCh38
NC_000011.9:g.2593071_2593072del , CM000673.1:g.2593071_2593072del	GRCh37
NC_000011.8:g.2549647_2549648del	NCBI36
NG_008935.1:g.131851_131852del , LRG_287:g.131851_131852del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.423-172_423-171del	ENSP00000434560.2:n.423-172_423-171del
ENST00000646564.2:c.478-11594_478-11593del	ENSP00000495806.2:n.478-11594_478-11593del
ENST00000155840.12:c.684-172_684-171del MANE Select	ENSP00000155840.2:n.684-172_684-171del
ENST00000335475.6:c.303-172_303-171del	ENSP00000334497.5:n.303-172_303-171del
ENST00000646564.1:c.124-11594_124-11593del	ENSP00000495806.1:n.124-11594_124-11593del
ENST00000155840.9:c.684-172_684-171del	ENSP00000155840.2:n.684-172_684-171del
ENST00000335475.5:c.303-172_303-171del	ENSP00000334497.5:n.303-172_303-171del
ENST00000496887.6:c.423-172_423-171del	ENSP00000434560.1:n.423-172_423-171del
NM_000218.2:c.684-172_684-171del , LRG_287t1:c.684-172_684-171del	NP_000209.2:n.684-172_684-171del
NM_181798.1:c.303-172_303-171del , LRG_287t2:c.303-172_303-171del	NP_861463.1:n.303-172_303-171del
NM_000218.3:c.684-172_684-171del MANE Select	NP_000209.2:n.684-172_684-171del