Canonical Allele Identifier: CA934472841
Gene: KCNQ1 HGNC NCBI

Linked Data

dbSNP Id: rs1845856402

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2731383_2731391del , CM000673.2:g.2731383_2731391del GRCh38
NC_000011.9:g.2752613_2752621del , CM000673.1:g.2752613_2752621del GRCh37
NC_000011.8:g.2709189_2709197del NCBI36
NG_008935.1:g.291393_291401del , LRG_287:g.291393_291401del

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.1158-37461_1158-37453del ENSP00000434560.2:n.1158-37461_1158-37453...
ENST00000646564.2:c.975-37461_975-37453del ENSP00000495806.2:n.975-37461_975-37453de...
ENST00000155840.12:c.1515-37461_1515-37453del MANE Select ENSP00000155840.2:n.1515-37461_1515-37453...
ENST00000335475.6:c.1134-37461_1134-37453del ENSP00000334497.5:n.1134-37461_1134-37453...
ENST00000646564.1:c.621-37461_621-37453del ENSP00000495806.1:n.621-37461_621-37453de...
ENST00000155840.9:c.1515-37461_1515-37453del ENSP00000155840.2:n.1515-37461_1515-37453...
ENST00000335475.5:c.1134-37461_1134-37453del ENSP00000334497.5:n.1134-37461_1134-37453...
NM_000218.2:c.1515-37461_1515-37453del , LRG_287t1:c.1515-37461_1515-37453del NP_000209.2:n.1515-37461_1515-37453del
NM_181798.1:c.1134-37461_1134-37453del , LRG_287t2:c.1134-37461_1134-37453del NP_861463.1:n.1134-37461_1134-37453del
NM_000218.3:c.1515-37461_1515-37453del MANE Select NP_000209.2:n.1515-37461_1515-37453del