Canonical Allele Identifier: CA379139032

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2790144T>G (hg19) ; chr11:g.2768914T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2768914T>G , CM000673.2:g.2768914T>G	GRCh38
NC_000011.9:g.2790144T>G , CM000673.1:g.2790144T>G	GRCh37
NC_000011.8:g.2746720T>G	NCBI36
NG_008935.1:g.328924T>G , LRG_287:g.328924T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1228T>G	ENSP00000434560.2:p.Phe410Val
ENST00000646564.2:c.1045T>G	ENSP00000495806.2:p.Phe349Val
ENST00000155840.12:c.1585T>G MANE Select	ENSP00000155840.2:p.Phe529Val
ENST00000335475.6:c.1204T>G	ENSP00000334497.5:p.Phe402Val
ENST00000646564.1:c.691T>G	ENSP00000495806.1:p.Phe231Val
ENST00000155840.9:c.1585T>G	ENSP00000155840.2:p.Phe529Val
ENST00000335475.5:c.1204T>G	ENSP00000334497.5:p.Phe402Val
NM_000218.2:c.1585T>G , LRG_287t1:c.1585T>G	NP_000209.2:p.Phe529Val
NM_181798.1:c.1204T>G , LRG_287t2:c.1204T>G	NP_861463.1:p.Phe402Val
NM_000218.3:c.1585T>G MANE Select	NP_000209.2:p.Phe529Val