Canonical Allele Identifier: CA379129871

Gene: KCNQ1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.259C>A	ENSP00000434560.2:p.Arg87Ser
ENST00000646564.2:c.478-12765C>A	ENSP00000495806.2:n.478-12765C>A
ENST00000155840.12:c.520C>A MANE Select	ENSP00000155840.2:p.Arg174Ser
ENST00000335475.6:c.139C>A	ENSP00000334497.5:p.Arg47Ser
ENST00000646564.1:c.124-12765C>A	ENSP00000495806.1:n.124-12765C>A
ENST00000155840.9:c.520C>A	ENSP00000155840.2:p.Arg174Ser
ENST00000335475.5:c.139C>A	ENSP00000334497.5:p.Arg47Ser
ENST00000496887.6:c.259C>A	ENSP00000434560.1:p.Arg87Ser
NM_000218.2:c.520C>A , LRG_287t1:c.520C>A	NP_000209.2:p.Arg174Ser
NM_181798.1:c.139C>A , LRG_287t2:c.139C>A	NP_861463.1:p.Arg47Ser
NM_000218.3:c.520C>A MANE Select	NP_000209.2:p.Arg174Ser