Canonical Allele Identifier: CA379117586

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2466669T>G (hg19) ; chr11:g.2445439T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2445439T>G , CM000673.2:g.2445439T>G	GRCh38
NC_000011.9:g.2466669T>G , CM000673.1:g.2466669T>G	GRCh37
NC_000011.8:g.2423245T>G	NCBI36
NG_008935.1:g.5449T>G , LRG_287:g.5449T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.80T>G	ENSP00000434560.2:p.Leu27Arg
ENST00000646564.2:c.341T>G	ENSP00000495806.2:p.Leu114Arg
ENST00000155840.12:c.341T>G MANE Select	ENSP00000155840.2:p.Leu114Arg
ENST00000155840.9:c.341T>G	ENSP00000155840.2:p.Leu114Arg
ENST00000345015.4:n.118T>G
ENST00000496887.6:c.80T>G	ENSP00000434560.1:p.Leu27Arg
NM_000218.2:c.341T>G , LRG_287t1:c.341T>G	NP_000209.2:p.Leu114Arg
NM_000218.3:c.341T>G MANE Select	NP_000209.2:p.Leu114Arg