Canonical Allele Identifier: CA379132995

Gene: KCNQ1

Linked Data

• ClinVar Variation Id: 1044172
• ClinVar RCV Id: RCV001348383
• dbSNP Id: rs1310931869
• MyVariant Identifiers: chr11:g.2604698G>A (hg19) ; chr11:g.2583468G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2583468G>A , CM000673.2:g.2583468G>A	GRCh38
NC_000011.9:g.2604698G>A , CM000673.1:g.2604698G>A	GRCh37
NC_000011.8:g.2561274G>A	NCBI36
NG_008935.1:g.143478G>A , LRG_287:g.143478G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.694G>A	ENSP00000434560.2:p.Val232Met
ENST00000646564.2:c.511G>A	ENSP00000495806.2:p.Val171Met
ENST00000155840.12:c.955G>A MANE Select	ENSP00000155840.2:p.Val319Met
ENST00000335475.6:c.574G>A	ENSP00000334497.5:p.Val192Met
ENST00000646564.1:c.157G>A	ENSP00000495806.1:p.Val53Met
ENST00000155840.9:c.955G>A	ENSP00000155840.2:p.Val319Met
ENST00000335475.5:c.574G>A	ENSP00000334497.5:p.Val192Met
NM_000218.2:c.955G>A , LRG_287t1:c.955G>A	NP_000209.2:p.Val319Met
NM_181798.1:c.574G>A , LRG_287t2:c.574G>A	NP_861463.1:p.Val192Met
NM_000218.3:c.955G>A MANE Select	NP_000209.2:p.Val319Met