Canonical Allele Identifier: CA916079942
Gene: KCNQ1 HGNC NCBI

Linked Data

ClinVar Variation Id: 861314
ClinVar RCV Id: RCV001067817
dbSNP Id: rs1848360153

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2572878_2572883del , CM000673.2:g.2572878_2572883del GRCh38
NC_000011.9:g.2594108_2594113del , CM000673.1:g.2594108_2594113del GRCh37
NC_000011.8:g.2550684_2550689del NCBI36
NG_008935.1:g.132888_132893del , LRG_287:g.132888_132893del

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.552_557del ENSP00000434560.2:p.Gly185_Leu186del
ENST00000646564.2:c.478-10557_478-10552del ENSP00000495806.2:n.478-10557_478-10552de...
ENST00000155840.12:c.813_818del MANE Select ENSP00000155840.2:p.Gly272_Leu273del
ENST00000335475.6:c.432_437del ENSP00000334497.5:p.Gly145_Leu146del
ENST00000646564.1:c.124-10557_124-10552del ENSP00000495806.1:n.124-10557_124-10552de...
ENST00000155840.9:c.813_818del ENSP00000155840.2:p.Gly272_Leu273del
ENST00000335475.5:c.432_437del ENSP00000334497.5:p.Gly145_Leu146del
ENST00000496887.6:c.552_557del ENSP00000434560.1:p.Gly185_Leu186del
NM_000218.2:c.813_818del , LRG_287t1:c.813_818del NP_000209.2:p.Gly272_Leu273del
NM_181798.1:c.432_437del , LRG_287t2:c.432_437del NP_861463.1:p.Gly145_Leu146del
NM_000218.3:c.813_818del MANE Select NP_000209.2:p.Gly272_Leu273del