Canonical Allele Identifier: CA379132993

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2604696A>T (hg19) ; chr11:g.2583466A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2583466A>T , CM000673.2:g.2583466A>T	GRCh38
NC_000011.9:g.2604696A>T , CM000673.1:g.2604696A>T	GRCh37
NC_000011.8:g.2561272A>T	NCBI36
NG_008935.1:g.143476A>T , LRG_287:g.143476A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.692A>T	ENSP00000434560.2:p.Lys231Met
ENST00000646564.2:c.509A>T	ENSP00000495806.2:p.Lys170Met
ENST00000155840.12:c.953A>T MANE Select	ENSP00000155840.2:p.Lys318Met
ENST00000335475.6:c.572A>T	ENSP00000334497.5:p.Lys191Met
ENST00000646564.1:c.155A>T	ENSP00000495806.1:p.Lys52Met
ENST00000155840.9:c.953A>T	ENSP00000155840.2:p.Lys318Met
ENST00000335475.5:c.572A>T	ENSP00000334497.5:p.Lys191Met
NM_000218.2:c.953A>T , LRG_287t1:c.953A>T	NP_000209.2:p.Lys318Met
NM_181798.1:c.572A>T , LRG_287t2:c.572A>T	NP_861463.1:p.Lys191Met
NM_000218.3:c.953A>T MANE Select	NP_000209.2:p.Lys318Met