Canonical Allele Identifier: CA472038127

Gene: KCNQ1

Linked Data

• gnomAD v4: 11-2572857-C-T
• MyVariant Identifiers: chr11:g.2594087C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2572857C>T , CM000673.2:g.2572857C>T	GRCh38
NC_000011.9:g.2594087C>T , CM000673.1:g.2594087C>T	GRCh37
NC_000011.8:g.2550663C>T	NCBI36
NG_008935.1:g.132867C>T , LRG_287:g.132867C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.531C>T	ENSP00000434560.2:p.Thr177=
ENST00000646564.2:c.478-10578C>T	ENSP00000495806.2:n.478-10578C>T
ENST00000155840.12:c.792C>T MANE Select	ENSP00000155840.2:p.Thr264=
ENST00000335475.6:c.411C>T	ENSP00000334497.5:p.Thr137=
ENST00000646564.1:c.124-10578C>T	ENSP00000495806.1:n.124-10578C>T
ENST00000155840.9:c.792C>T	ENSP00000155840.2:p.Thr264=
ENST00000335475.5:c.411C>T	ENSP00000334497.5:p.Thr137=
ENST00000496887.6:c.531C>T	ENSP00000434560.1:p.Thr177=
NM_000218.2:c.792C>T , LRG_287t1:c.792C>T	NP_000209.2:p.Thr264=
NM_181798.1:c.411C>T , LRG_287t2:c.411C>T	NP_861463.1:p.Thr137=
NM_000218.3:c.792C>T MANE Select	NP_000209.2:p.Thr264=