Canonical Allele Identifier: CA379131061

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2593325T>A (hg19) ; chr11:g.2572095T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2572095T>A , CM000673.2:g.2572095T>A	GRCh38
NC_000011.9:g.2593325T>A , CM000673.1:g.2593325T>A	GRCh37
NC_000011.8:g.2549901T>A	NCBI36
NG_008935.1:g.132105T>A , LRG_287:g.132105T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.505T>A	ENSP00000434560.2:p.Phe169Ile
ENST00000646564.2:c.478-11340T>A	ENSP00000495806.2:n.478-11340T>A
ENST00000155840.12:c.766T>A MANE Select	ENSP00000155840.2:p.Phe256Ile
ENST00000335475.6:c.385T>A	ENSP00000334497.5:p.Phe129Ile
ENST00000646564.1:c.124-11340T>A	ENSP00000495806.1:n.124-11340T>A
ENST00000155840.9:c.766T>A	ENSP00000155840.2:p.Phe256Ile
ENST00000335475.5:c.385T>A	ENSP00000334497.5:p.Phe129Ile
ENST00000496887.6:c.505T>A	ENSP00000434560.1:p.Phe169Ile
NM_000218.2:c.766T>A , LRG_287t1:c.766T>A	NP_000209.2:p.Phe256Ile
NM_181798.1:c.385T>A , LRG_287t2:c.385T>A	NP_861463.1:p.Phe129Ile
NM_000218.3:c.766T>A MANE Select	NP_000209.2:p.Phe256Ile