Canonical Allele Identifier: CA472038241

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2549200C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2527970C>G , CM000673.2:g.2527970C>G	GRCh38
NC_000011.9:g.2549200C>G , CM000673.1:g.2549200C>G	GRCh37
NC_000011.8:g.2505776C>G	NCBI36
NG_008935.1:g.87980C>G , LRG_287:g.87980C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000380776.5:n.226C>G
ENST00000496887.7:c.168C>G	ENSP00000434560.2:p.Ser56=
ENST00000646564.2:c.429C>G	ENSP00000495806.2:p.Ser143=
ENST00000155840.12:c.429C>G MANE Select	ENSP00000155840.2:p.Ser143=
ENST00000335475.6:c.48C>G	ENSP00000334497.5:p.Ser16=
ENST00000646564.1:c.75C>G	ENSP00000495806.1:p.Ser25=
ENST00000155840.9:c.429C>G	ENSP00000155840.2:p.Ser143=
ENST00000335475.5:c.48C>G	ENSP00000334497.5:p.Ser16=
ENST00000345015.4:n.298C>G
ENST00000380776.4:c.219C>G	ENSP00000370153.4:p.Ser73=
ENST00000496887.6:c.168C>G	ENSP00000434560.1:p.Ser56=
NM_000218.2:c.429C>G , LRG_287t1:c.429C>G	NP_000209.2:p.Ser143=
NM_181798.1:c.48C>G , LRG_287t2:c.48C>G	NP_861463.1:p.Ser16=
NM_000218.3:c.429C>G MANE Select	NP_000209.2:p.Ser143=