Canonical Allele Identifier: CA2574728367
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2572752del , CM000673.2:g.2572752del GRCh38
NC_000011.9:g.2593982del , CM000673.1:g.2593982del GRCh37
NC_000011.8:g.2550558del NCBI36
NG_008935.1:g.132762del , LRG_287:g.132762del

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.520-94del ENSP00000434560.2:n.520-94del
ENST00000646564.2:c.478-10683del ENSP00000495806.2:n.478-10683del
ENST00000155840.12:c.781-94del MANE Select ENSP00000155840.2:n.781-94del
ENST00000335475.6:c.400-94del ENSP00000334497.5:n.400-94del
ENST00000646564.1:c.124-10683del ENSP00000495806.1:n.124-10683del
ENST00000155840.9:c.781-94del ENSP00000155840.2:n.781-94del
ENST00000335475.5:c.400-94del ENSP00000334497.5:n.400-94del
ENST00000496887.6:c.520-94del ENSP00000434560.1:n.520-94del
NM_000218.2:c.781-94del , LRG_287t1:c.781-94del NP_000209.2:n.781-94del
NM_181798.1:c.400-94del , LRG_287t2:c.400-94del NP_861463.1:n.400-94del
NM_000218.3:c.781-94del MANE Select NP_000209.2:n.781-94del