Canonical Allele Identifier: CA379131003

Gene: KCNQ1

Linked Data

• ClinVar Variation Id: 855976
• ClinVar RCV Id: RCV001061339
• dbSNP Id: rs1848344878
• MyVariant Identifiers: chr11:g.2593302G>A (hg19) ; chr11:g.2572072G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2572072G>A , CM000673.2:g.2572072G>A	GRCh38
NC_000011.9:g.2593302G>A , CM000673.1:g.2593302G>A	GRCh37
NC_000011.8:g.2549878G>A	NCBI36
NG_008935.1:g.132082G>A , LRG_287:g.132082G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.482G>A	ENSP00000434560.2:p.Trp161Ter
ENST00000646564.2:c.478-11363G>A	ENSP00000495806.2:n.478-11363G>A
ENST00000155840.12:c.743G>A MANE Select	ENSP00000155840.2:p.Trp248Ter
ENST00000335475.6:c.362G>A	ENSP00000334497.5:p.Trp121Ter
ENST00000646564.1:c.124-11363G>A	ENSP00000495806.1:n.124-11363G>A
ENST00000155840.9:c.743G>A	ENSP00000155840.2:p.Trp248Ter
ENST00000335475.5:c.362G>A	ENSP00000334497.5:p.Trp121Ter
ENST00000496887.6:c.482G>A	ENSP00000434560.1:p.Trp161Ter
NM_000218.2:c.743G>A , LRG_287t1:c.743G>A	NP_000209.2:p.Trp248Ter
NM_181798.1:c.362G>A , LRG_287t2:c.362G>A	NP_861463.1:p.Trp121Ter
NM_000218.3:c.743G>A MANE Select	NP_000209.2:p.Trp248Ter