Canonical Allele Identifier: CA379130607

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2592605G>T (hg19) ; chr11:g.2571375G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2571375G>T , CM000673.2:g.2571375G>T	GRCh38
NC_000011.9:g.2592605G>T , CM000673.1:g.2592605G>T	GRCh37
NC_000011.8:g.2549181G>T	NCBI36
NG_008935.1:g.131385G>T , LRG_287:g.131385G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.394G>T	ENSP00000434560.2:p.Gly132Trp
ENST00000646564.2:c.478-12060G>T	ENSP00000495806.2:n.478-12060G>T
ENST00000155840.12:c.655G>T MANE Select	ENSP00000155840.2:p.Gly219Trp
ENST00000335475.6:c.274G>T	ENSP00000334497.5:p.Gly92Trp
ENST00000646564.1:c.124-12060G>T	ENSP00000495806.1:n.124-12060G>T
ENST00000155840.9:c.655G>T	ENSP00000155840.2:p.Gly219Trp
ENST00000335475.5:c.274G>T	ENSP00000334497.5:p.Gly92Trp
ENST00000496887.6:c.394G>T	ENSP00000434560.1:p.Gly132Trp
NM_000218.2:c.655G>T , LRG_287t1:c.655G>T	NP_000209.2:p.Gly219Trp
NM_181798.1:c.274G>T , LRG_287t2:c.274G>T	NP_861463.1:p.Gly92Trp
NM_000218.3:c.655G>T MANE Select	NP_000209.2:p.Gly219Trp