Canonical Allele Identifier: CA472459426

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2790080G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2768850G>T , CM000673.2:g.2768850G>T	GRCh38
NC_000011.9:g.2790080G>T , CM000673.1:g.2790080G>T	GRCh37
NC_000011.8:g.2746656G>T	NCBI36
NG_008935.1:g.328860G>T , LRG_287:g.328860G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1164G>T	ENSP00000434560.2:p.Arg388=
ENST00000646564.2:c.981G>T	ENSP00000495806.2:p.Arg327=
ENST00000155840.12:c.1521G>T MANE Select	ENSP00000155840.2:p.Arg507=
ENST00000335475.6:c.1140G>T	ENSP00000334497.5:p.Arg380=
ENST00000646564.1:c.627G>T	ENSP00000495806.1:p.Arg209=
ENST00000155840.9:c.1521G>T	ENSP00000155840.2:p.Arg507=
ENST00000335475.5:c.1140G>T	ENSP00000334497.5:p.Arg380=
NM_000218.2:c.1521G>T , LRG_287t1:c.1521G>T	NP_000209.2:p.Arg507=
NM_181798.1:c.1140G>T , LRG_287t2:c.1140G>T	NP_861463.1:p.Arg380=
NM_000218.3:c.1521G>T MANE Select	NP_000209.2:p.Arg507=