Canonical Allele Identifier: CA472039843

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2610014C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2588784C>G , CM000673.2:g.2588784C>G	GRCh38
NC_000011.9:g.2610014C>G , CM000673.1:g.2610014C>G	GRCh37
NC_000011.8:g.2566590C>G	NCBI36
NG_008935.1:g.148794C>G , LRG_287:g.148794C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.966C>G	ENSP00000434560.2:p.Pro322=
ENST00000646564.2:c.783C>G	ENSP00000495806.2:p.Pro261=
ENST00000155840.12:c.1323C>G MANE Select	ENSP00000155840.2:p.Pro441=
ENST00000335475.6:c.942C>G	ENSP00000334497.5:p.Pro314=
ENST00000646564.1:c.429C>G	ENSP00000495806.1:p.Pro143=
ENST00000155840.9:c.1323C>G	ENSP00000155840.2:p.Pro441=
ENST00000335475.5:c.942C>G	ENSP00000334497.5:p.Pro314=
NM_000218.2:c.1323C>G , LRG_287t1:c.1323C>G	NP_000209.2:p.Pro441=
NM_181798.1:c.942C>G , LRG_287t2:c.942C>G	NP_861463.1:p.Pro314=
NM_000218.3:c.1323C>G MANE Select	NP_000209.2:p.Pro441=