Canonical Allele Identifier: CA658761314
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2445340_2445362delinsGCGCCCGCGG , CM000673.2:g.2445340_2445362delinsGCGCCCGCGG GRCh38
NC_000011.9:g.2466570_2466592delinsGCGCCCGCGG , CM000673.1:g.2466570_2466592delinsGCGCCCGCGG GRCh37
NC_000011.8:g.2423146_2423168delinsGCGCCCGCGG NCBI36
NG_008935.1:g.5350_5372delinsGCGCCCGCGG , LRG_287:g.5350_5372delinsGCGCCCGCGG

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.24-43_24-21delinsGCGCCCGCGG ENSP00000434560.2:n.24-43_24-21delinsGCGC...
ENST00000646564.2:c.242_264delinsGCGCCCGCGG ENSP00000495806.2:p.Pro81ArgfsTer?
ENST00000155840.12:c.242_264delinsGCGCCCGCGG MANE Select ENSP00000155840.2:p.Pro81ArgfsTer?
ENST00000155840.9:c.242_264delinsGCGCCCGCGG ENSP00000155840.2:p.Pro81ArgfsTer?
ENST00000345015.4:n.19_41delinsGCGCCCGCGG
ENST00000496887.6:c.24-43_24-21delinsGCGCCCGCGG ENSP00000434560.1:n.24-43_24-21delinsGCGC...
NM_000218.2:c.242_264delinsGCGCCCGCGG , LRG_287t1:c.242_264delinsGCGCCCGCGG NP_000209.2:p.Pro81ArgfsTer?
NM_000218.3:c.242_264delinsGCGCCCGCGG MANE Select NP_000209.2:p.Pro81ArgfsTer?