Canonical Allele Identifier: CA2697558822

Gene: KCNQ1

Linked Data

• ClinVar Variation Id: 2773461
• ClinVar RCV Id: RCV003592286

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2527924G>T , CM000673.2:g.2527924G>T	GRCh38
NC_000011.9:g.2549154G>T , CM000673.1:g.2549154G>T	GRCh37
NC_000011.8:g.2505730G>T	NCBI36
NG_008935.1:g.87934G>T , LRG_287:g.87934G>T

Transcript Alleles

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