Canonical Allele Identifier: CA472039922

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2610045C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2588815C>A , CM000673.2:g.2588815C>A	GRCh38
NC_000011.9:g.2610045C>A , CM000673.1:g.2610045C>A	GRCh37
NC_000011.8:g.2566621C>A	NCBI36
NG_008935.1:g.148825C>A , LRG_287:g.148825C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.997C>A	ENSP00000434560.2:p.Arg333=
ENST00000646564.2:c.814C>A	ENSP00000495806.2:p.Arg272=
ENST00000155840.12:c.1354C>A MANE Select	ENSP00000155840.2:p.Arg452=
ENST00000335475.6:c.973C>A	ENSP00000334497.5:p.Arg325=
ENST00000646564.1:c.460C>A	ENSP00000495806.1:p.Arg154=
ENST00000155840.9:c.1354C>A	ENSP00000155840.2:p.Arg452=
ENST00000335475.5:c.973C>A	ENSP00000334497.5:p.Arg325=
NM_000218.2:c.1354C>A , LRG_287t1:c.1354C>A	NP_000209.2:p.Arg452=
NM_181798.1:c.973C>A , LRG_287t2:c.973C>A	NP_861463.1:p.Arg325=
NM_000218.3:c.1354C>A MANE Select	NP_000209.2:p.Arg452=