Canonical Allele Identifier: CA379130959

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2593277C>T (hg19) ; chr11:g.2572047C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2572047C>T , CM000673.2:g.2572047C>T	GRCh38
NC_000011.9:g.2593277C>T , CM000673.1:g.2593277C>T	GRCh37
NC_000011.8:g.2549853C>T	NCBI36
NG_008935.1:g.132057C>T , LRG_287:g.132057C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.457C>T	ENSP00000434560.2:p.His153Tyr
ENST00000646564.2:c.478-11388C>T	ENSP00000495806.2:n.478-11388C>T
ENST00000155840.12:c.718C>T MANE Select	ENSP00000155840.2:p.His240Tyr
ENST00000335475.6:c.337C>T	ENSP00000334497.5:p.His113Tyr
ENST00000646564.1:c.124-11388C>T	ENSP00000495806.1:n.124-11388C>T
ENST00000155840.9:c.718C>T	ENSP00000155840.2:p.His240Tyr
ENST00000335475.5:c.337C>T	ENSP00000334497.5:p.His113Tyr
ENST00000496887.6:c.457C>T	ENSP00000434560.1:p.His153Tyr
NM_000218.2:c.718C>T , LRG_287t1:c.718C>T	NP_000209.2:p.His240Tyr
NM_181798.1:c.337C>T , LRG_287t2:c.337C>T	NP_861463.1:p.His113Tyr
NM_000218.3:c.718C>T MANE Select	NP_000209.2:p.His240Tyr