Canonical Allele Identifier: CA472038216

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2549167C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2527937C>A , CM000673.2:g.2527937C>A	GRCh38
NC_000011.9:g.2549167C>A , CM000673.1:g.2549167C>A	GRCh37
NC_000011.8:g.2505743C>A	NCBI36
NG_008935.1:g.87947C>A , LRG_287:g.87947C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000380776.5:n.193C>A
ENST00000496887.7:c.135C>A	ENSP00000434560.2:p.Ile45=
ENST00000646564.2:c.396C>A	ENSP00000495806.2:p.Ile132=
ENST00000155840.12:c.396C>A MANE Select	ENSP00000155840.2:p.Ile132=
ENST00000335475.6:c.15C>A	ENSP00000334497.5:p.Ile5=
ENST00000646564.1:c.42C>A	ENSP00000495806.1:p.Ile14=
ENST00000155840.9:c.396C>A	ENSP00000155840.2:p.Ile132=
ENST00000335475.5:c.15C>A	ENSP00000334497.5:p.Ile5=
ENST00000345015.4:n.265C>A
ENST00000380776.4:c.186C>A	ENSP00000370153.4:p.Ile62=
ENST00000496887.6:c.135C>A	ENSP00000434560.1:p.Ile45=
NM_000218.2:c.396C>A , LRG_287t1:c.396C>A	NP_000209.2:p.Ile132=
NM_181798.1:c.15C>A , LRG_287t2:c.15C>A	NP_861463.1:p.Ile5=
NM_000218.3:c.396C>A MANE Select	NP_000209.2:p.Ile132=