Canonical Allele Identifier: CA379131027

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2593314G>T (hg19) ; chr11:g.2572084G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2572084G>T , CM000673.2:g.2572084G>T	GRCh38
NC_000011.9:g.2593314G>T , CM000673.1:g.2593314G>T	GRCh37
NC_000011.8:g.2549890G>T	NCBI36
NG_008935.1:g.132094G>T , LRG_287:g.132094G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.494G>T	ENSP00000434560.2:p.Gly165Val
ENST00000646564.2:c.478-11351G>T	ENSP00000495806.2:n.478-11351G>T
ENST00000155840.12:c.755G>T MANE Select	ENSP00000155840.2:p.Gly252Val
ENST00000335475.6:c.374G>T	ENSP00000334497.5:p.Gly125Val
ENST00000646564.1:c.124-11351G>T	ENSP00000495806.1:n.124-11351G>T
ENST00000155840.9:c.755G>T	ENSP00000155840.2:p.Gly252Val
ENST00000335475.5:c.374G>T	ENSP00000334497.5:p.Gly125Val
ENST00000496887.6:c.494G>T	ENSP00000434560.1:p.Gly165Val
NM_000218.2:c.755G>T , LRG_287t1:c.755G>T	NP_000209.2:p.Gly252Val
NM_181798.1:c.374G>T , LRG_287t2:c.374G>T	NP_861463.1:p.Gly125Val
NM_000218.3:c.755G>T MANE Select	NP_000209.2:p.Gly252Val