Canonical Allele Identifier: CA379129872

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2591900C>G (hg19) ; chr11:g.2570670C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2570670C>G , CM000673.2:g.2570670C>G	GRCh38
NC_000011.9:g.2591900C>G , CM000673.1:g.2591900C>G	GRCh37
NC_000011.8:g.2548476C>G	NCBI36
NG_008935.1:g.130680C>G , LRG_287:g.130680C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.259C>G	ENSP00000434560.2:p.Arg87Gly
ENST00000646564.2:c.478-12765C>G	ENSP00000495806.2:n.478-12765C>G
ENST00000155840.12:c.520C>G MANE Select	ENSP00000155840.2:p.Arg174Gly
ENST00000335475.6:c.139C>G	ENSP00000334497.5:p.Arg47Gly
ENST00000646564.1:c.124-12765C>G	ENSP00000495806.1:n.124-12765C>G
ENST00000155840.9:c.520C>G	ENSP00000155840.2:p.Arg174Gly
ENST00000335475.5:c.139C>G	ENSP00000334497.5:p.Arg47Gly
ENST00000496887.6:c.259C>G	ENSP00000434560.1:p.Arg87Gly
NM_000218.2:c.520C>G , LRG_287t1:c.520C>G	NP_000209.2:p.Arg174Gly
NM_181798.1:c.139C>G , LRG_287t2:c.139C>G	NP_861463.1:p.Arg47Gly
NM_000218.3:c.520C>G MANE Select	NP_000209.2:p.Arg174Gly