Canonical Allele Identifier: CA472038260

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2549221C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2527991C>G , CM000673.2:g.2527991C>G	GRCh38
NC_000011.9:g.2549221C>G , CM000673.1:g.2549221C>G	GRCh37
NC_000011.8:g.2505797C>G	NCBI36
NG_008935.1:g.88001C>G , LRG_287:g.88001C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.189C>G	ENSP00000434560.2:p.Ala63=
ENST00000646564.2:c.450C>G	ENSP00000495806.2:p.Ala150=
ENST00000155840.12:c.450C>G MANE Select	ENSP00000155840.2:p.Ala150=
ENST00000335475.6:c.69C>G	ENSP00000334497.5:p.Ala23=
ENST00000646564.1:c.96C>G	ENSP00000495806.1:p.Ala32=
ENST00000155840.9:c.450C>G	ENSP00000155840.2:p.Ala150=
ENST00000335475.5:c.69C>G	ENSP00000334497.5:p.Ala23=
ENST00000496887.6:c.189C>G	ENSP00000434560.1:p.Ala63=
NM_000218.2:c.450C>G , LRG_287t1:c.450C>G	NP_000209.2:p.Ala150=
NM_181798.1:c.69C>G , LRG_287t2:c.69C>G	NP_861463.1:p.Ala23=
NM_000218.3:c.450C>G MANE Select	NP_000209.2:p.Ala150=