Canonical Allele Identifier: CA2612008558
Gene: KCNQ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2768809del , CM000673.2:g.2768809del GRCh38
NC_000011.9:g.2790039del , CM000673.1:g.2790039del GRCh37
NC_000011.8:g.2746615del NCBI36
NG_008935.1:g.328819del , LRG_287:g.328819del

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.1158-35del ENSP00000434560.2:n.1158-35del
ENST00000646564.2:c.975-35del ENSP00000495806.2:n.975-35del
ENST00000155840.12:c.1515-35del MANE Select ENSP00000155840.2:n.1515-35del
ENST00000335475.6:c.1134-35del ENSP00000334497.5:n.1134-35del
ENST00000646564.1:c.621-35del ENSP00000495806.1:n.621-35del
ENST00000155840.9:c.1515-35del ENSP00000155840.2:n.1515-35del
ENST00000335475.5:c.1134-35del ENSP00000334497.5:n.1134-35del
NM_000218.2:c.1515-35del , LRG_287t1:c.1515-35del NP_000209.2:n.1515-35del
NM_181798.1:c.1134-35del , LRG_287t2:c.1134-35del NP_861463.1:n.1134-35del
NM_000218.3:c.1515-35del MANE Select NP_000209.2:n.1515-35del