Canonical Allele Identifier: CA379138914

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2790085A>T (hg19) ; chr11:g.2768855A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2768855A>T , CM000673.2:g.2768855A>T	GRCh38
NC_000011.9:g.2790085A>T , CM000673.1:g.2790085A>T	GRCh37
NC_000011.8:g.2746661A>T	NCBI36
NG_008935.1:g.328865A>T , LRG_287:g.328865A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1169A>T	ENSP00000434560.2:p.His390Leu
ENST00000646564.2:c.986A>T	ENSP00000495806.2:p.His329Leu
ENST00000155840.12:c.1526A>T MANE Select	ENSP00000155840.2:p.His509Leu
ENST00000335475.6:c.1145A>T	ENSP00000334497.5:p.His382Leu
ENST00000646564.1:c.632A>T	ENSP00000495806.1:p.His211Leu
ENST00000155840.9:c.1526A>T	ENSP00000155840.2:p.His509Leu
ENST00000335475.5:c.1145A>T	ENSP00000334497.5:p.His382Leu
NM_000218.2:c.1526A>T , LRG_287t1:c.1526A>T	NP_000209.2:p.His509Leu
NM_181798.1:c.1145A>T , LRG_287t2:c.1145A>T	NP_861463.1:p.His382Leu
NM_000218.3:c.1526A>T MANE Select	NP_000209.2:p.His509Leu