Canonical Allele Identifier: CA675121273

Gene: KCNQ1

Linked Data

• dbSNP Id: rs1336381371
• gnomAD v3: 11-2731316-ACAATGCCC-A
• gnomAD v4: 11-2731316-ACAATGCCC-A
• MyVariant Identifiers: chr11:g.2752547_2752554del (hg19) ; chr11:g.2731317_2731324del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2731317_2731324del , CM000673.2:g.2731317_2731324del	GRCh38
NC_000011.9:g.2752547_2752554del , CM000673.1:g.2752547_2752554del	GRCh37
NC_000011.8:g.2709123_2709130del	NCBI36
NG_008935.1:g.291327_291334del , LRG_287:g.291327_291334del

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.1158-37527_1158-37520del	ENSP00000434560.2:n.1158-37527_1158-37520del
ENST00000646564.2:c.975-37527_975-37520del	ENSP00000495806.2:n.975-37527_975-37520del
ENST00000155840.12:c.1515-37527_1515-37520del MANE Select	ENSP00000155840.2:n.1515-37527_1515-37520del
ENST00000335475.6:c.1134-37527_1134-37520del	ENSP00000334497.5:n.1134-37527_1134-37520del
ENST00000646564.1:c.621-37527_621-37520del	ENSP00000495806.1:n.621-37527_621-37520del
ENST00000155840.9:c.1515-37527_1515-37520del	ENSP00000155840.2:n.1515-37527_1515-37520del
ENST00000335475.5:c.1134-37527_1134-37520del	ENSP00000334497.5:n.1134-37527_1134-37520del
NM_000218.2:c.1515-37527_1515-37520del , LRG_287t1:c.1515-37527_1515-37520del	NP_000209.2:n.1515-37527_1515-37520del
NM_181798.1:c.1134-37527_1134-37520del , LRG_287t2:c.1134-37527_1134-37520del	NP_861463.1:n.1134-37527_1134-37520del
NM_000218.3:c.1515-37527_1515-37520del MANE Select	NP_000209.2:n.1515-37527_1515-37520del