Canonical Allele Identifier: CA2611999937
Gene: KCNQ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2445174_2445175del , CM000673.2:g.2445174_2445175del GRCh38
NC_000011.9:g.2466404_2466405del , CM000673.1:g.2466404_2466405del GRCh37
NC_000011.8:g.2422980_2422981del NCBI36
NG_008935.1:g.5184_5185del , LRG_287:g.5184_5185del

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.24-209_24-208del ENSP00000434560.2:n.24-209_24-208del
ENST00000646564.2:c.76_77del ENSP00000495806.2:p.Gly26GlnfsTer?
ENST00000155840.12:c.76_77del MANE Select ENSP00000155840.2:p.Gly26GlnfsTer?
ENST00000155840.9:c.76_77del ENSP00000155840.2:p.Gly26GlnfsTer?
ENST00000496887.6:c.24-209_24-208del ENSP00000434560.1:n.24-209_24-208del
NM_000218.2:c.76_77del , LRG_287t1:c.76_77del NP_000209.2:p.Gly26GlnfsTer?
NM_000218.3:c.76_77del MANE Select NP_000209.2:p.Gly26GlnfsTer?