Canonical Allele Identifier: CA472037802

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2591899C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2570669C>G , CM000673.2:g.2570669C>G	GRCh38
NC_000011.9:g.2591899C>G , CM000673.1:g.2591899C>G	GRCh37
NC_000011.8:g.2548475C>G	NCBI36
NG_008935.1:g.130679C>G , LRG_287:g.130679C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.258C>G	ENSP00000434560.2:p.Val86=
ENST00000646564.2:c.478-12766C>G	ENSP00000495806.2:n.478-12766C>G
ENST00000155840.12:c.519C>G MANE Select	ENSP00000155840.2:p.Val173=
ENST00000335475.6:c.138C>G	ENSP00000334497.5:p.Val46=
ENST00000646564.1:c.124-12766C>G	ENSP00000495806.1:n.124-12766C>G
ENST00000155840.9:c.519C>G	ENSP00000155840.2:p.Val173=
ENST00000335475.5:c.138C>G	ENSP00000334497.5:p.Val46=
ENST00000496887.6:c.258C>G	ENSP00000434560.1:p.Val86=
NM_000218.2:c.519C>G , LRG_287t1:c.519C>G	NP_000209.2:p.Val173=
NM_181798.1:c.138C>G , LRG_287t2:c.138C>G	NP_861463.1:p.Val46=
NM_000218.3:c.519C>G MANE Select	NP_000209.2:p.Val173=