Canonical Allele Identifier: CA379138981

Gene: KCNQ1

Linked Data

• dbSNP Id: rs1846543207
• MyVariant Identifiers: chr11:g.2790121A>G (hg19) ; chr11:g.2768891A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2768891A>G , CM000673.2:g.2768891A>G	GRCh38
NC_000011.9:g.2790121A>G , CM000673.1:g.2790121A>G	GRCh37
NC_000011.8:g.2746697A>G	NCBI36
NG_008935.1:g.328901A>G , LRG_287:g.328901A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1205A>G	ENSP00000434560.2:p.Gln402Arg
ENST00000646564.2:c.1022A>G	ENSP00000495806.2:p.Gln341Arg
ENST00000155840.12:c.1562A>G MANE Select	ENSP00000155840.2:p.Gln521Arg
ENST00000335475.6:c.1181A>G	ENSP00000334497.5:p.Gln394Arg
ENST00000646564.1:c.668A>G	ENSP00000495806.1:p.Gln223Arg
ENST00000155840.9:c.1562A>G	ENSP00000155840.2:p.Gln521Arg
ENST00000335475.5:c.1181A>G	ENSP00000334497.5:p.Gln394Arg
NM_000218.2:c.1562A>G , LRG_287t1:c.1562A>G	NP_000209.2:p.Gln521Arg
NM_181798.1:c.1181A>G , LRG_287t2:c.1181A>G	NP_861463.1:p.Gln394Arg
NM_000218.3:c.1562A>G MANE Select	NP_000209.2:p.Gln521Arg