Canonical Allele Identifier: CA2695213145
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2570705_2570710del , CM000673.2:g.2570705_2570710del GRCh38
NC_000011.9:g.2591935_2591940del , CM000673.1:g.2591935_2591940del GRCh37
NC_000011.8:g.2548511_2548516del NCBI36
NG_008935.1:g.130715_130720del , LRG_287:g.130715_130720del

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.294_299del ENSP00000434560.2:p.Gly99_Leu100del
ENST00000646564.2:c.478-12730_478-12725del ENSP00000495806.2:n.478-12730_478-12725de...
ENST00000155840.12:c.555_560del MANE Select ENSP00000155840.2:p.Gly186_Leu187del
ENST00000335475.6:c.174_179del ENSP00000334497.5:p.Gly59_Leu60del
ENST00000646564.1:c.124-12730_124-12725del ENSP00000495806.1:n.124-12730_124-12725de...
ENST00000155840.9:c.555_560del ENSP00000155840.2:p.Gly186_Leu187del
ENST00000335475.5:c.174_179del ENSP00000334497.5:p.Gly59_Leu60del
ENST00000496887.6:c.294_299del ENSP00000434560.1:p.Gly99_Leu100del
NM_000218.2:c.555_560del , LRG_287t1:c.555_560del NP_000209.2:p.Gly186_Leu187del
NM_181798.1:c.174_179del , LRG_287t2:c.174_179del NP_861463.1:p.Gly59_Leu60del
NM_000218.3:c.555_560del MANE Select NP_000209.2:p.Gly186_Leu187del