Canonical Allele Identifier: CA379131800

Gene: KCNQ1

Linked Data

• dbSNP Id: rs1589958619
• MyVariant Identifiers: chr11:g.2594215T>G (hg19) ; chr11:g.2572985T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2572985T>G , CM000673.2:g.2572985T>G	GRCh38
NC_000011.9:g.2594215T>G , CM000673.1:g.2594215T>G	GRCh37
NC_000011.8:g.2550791T>G	NCBI36
NG_008935.1:g.132995T>G , LRG_287:g.132995T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.659T>G	ENSP00000434560.2:p.Val220Gly
ENST00000646564.2:c.478-10450T>G	ENSP00000495806.2:n.478-10450T>G
ENST00000155840.12:c.920T>G MANE Select	ENSP00000155840.2:p.Val307Gly
ENST00000335475.6:c.539T>G	ENSP00000334497.5:p.Val180Gly
ENST00000646564.1:c.124-10450T>G	ENSP00000495806.1:n.124-10450T>G
ENST00000155840.9:c.920T>G	ENSP00000155840.2:p.Val307Gly
ENST00000335475.5:c.539T>G	ENSP00000334497.5:p.Val180Gly
NM_000218.2:c.920T>G , LRG_287t1:c.920T>G	NP_000209.2:p.Val307Gly
NM_181798.1:c.539T>G , LRG_287t2:c.539T>G	NP_861463.1:p.Val180Gly
NM_000218.3:c.920T>G MANE Select	NP_000209.2:p.Val307Gly