Canonical Allele Identifier: CA934461589

Gene: KCNQ1

Linked Data

• dbSNP Id: rs1847536353
• gnomAD v3: 11-2527825-CT-C
• gnomAD v4: 11-2527825-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2527826del , CM000673.2:g.2527826del	GRCh38
NC_000011.9:g.2549056del , CM000673.1:g.2549056del	GRCh37
NC_000011.8:g.2505632del	NCBI36
NG_008935.1:g.87836del , LRG_287:g.87836del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380776.5:n.184-102del
ENST00000496887.7:c.126-102del	ENSP00000434560.2:n.126-102del
ENST00000646564.2:c.387-102del	ENSP00000495806.2:n.387-102del
ENST00000155840.12:c.387-102del MANE Select	ENSP00000155840.2:n.387-102del
ENST00000335475.6:c.6-102del	ENSP00000334497.5:n.6-102del
ENST00000646564.1:c.33-102del	ENSP00000495806.1:n.33-102del
ENST00000155840.9:c.387-102del	ENSP00000155840.2:n.387-102del
ENST00000335475.5:c.6-102del	ENSP00000334497.5:n.6-102del
ENST00000345015.4:n.256-102del
ENST00000380776.4:c.177-102del	ENSP00000370153.4:n.177-102del
ENST00000496887.6:c.126-102del	ENSP00000434560.1:n.126-102del
NM_000218.2:c.387-102del , LRG_287t1:c.387-102del	NP_000209.2:n.387-102del
NM_181798.1:c.6-102del , LRG_287t2:c.6-102del	NP_861463.1:n.6-102del
NM_000218.3:c.387-102del MANE Select	NP_000209.2:n.387-102del