Canonical Allele Identifier: CA2574728440
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2768947del , CM000673.2:g.2768947del GRCh38
NC_000011.9:g.2790177del , CM000673.1:g.2790177del GRCh37
NC_000011.8:g.2746753del NCBI36
NG_008935.1:g.328957del , LRG_287:g.328957del

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.1233+28del ENSP00000434560.2:n.1233+28del
ENST00000646564.2:c.1050+28del ENSP00000495806.2:n.1050+28del
ENST00000155840.12:c.1590+28del MANE Select ENSP00000155840.2:n.1590+28del
ENST00000335475.6:c.1209+28del ENSP00000334497.5:n.1209+28del
ENST00000646564.1:c.696+28del ENSP00000495806.1:n.696+28del
ENST00000155840.9:c.1590+28del ENSP00000155840.2:n.1590+28del
ENST00000335475.5:c.1209+28del ENSP00000334497.5:n.1209+28del
NM_000218.2:c.1590+28del , LRG_287t1:c.1590+28del NP_000209.2:n.1590+28del
NM_181798.1:c.1209+28del , LRG_287t2:c.1209+28del NP_861463.1:n.1209+28del
NM_000218.3:c.1590+28del MANE Select NP_000209.2:n.1590+28del