Canonical Allele Identifier: CA008541

Gene: KCNQ1

Linked Data

• ClinVar Variation Id: 67119
• ClinVar RCV Id: RCV000057787 ; RCV001044347
• dbSNP Id: rs199472738
• MyVariant Identifiers: chr11:g.2594182T>C (hg19) ; chr11:g.2572952T>C (hg38)
• PubMed: PMID:17470695 ; PMID:17905336 ; PMID:22581653

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2572952T>C , CM000673.2:g.2572952T>C	GRCh38
NC_000011.9:g.2594182T>C , CM000673.1:g.2594182T>C	GRCh37
NC_000011.8:g.2550758T>C	NCBI36
NG_008935.1:g.132962T>C , LRG_287:g.132962T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.626T>C	ENSP00000434560.2:p.Phe209Ser
ENST00000646564.2:c.478-10483T>C	ENSP00000495806.2:n.478-10483T>C
ENST00000155840.12:c.887T>C MANE Select	ENSP00000155840.2:p.Phe296Ser
ENST00000335475.6:c.506T>C	ENSP00000334497.5:p.Phe169Ser
ENST00000646564.1:c.124-10483T>C	ENSP00000495806.1:n.124-10483T>C
ENST00000155840.9:c.887T>C	ENSP00000155840.2:p.Phe296Ser
ENST00000335475.5:c.506T>C	ENSP00000334497.5:p.Phe169Ser
NM_000218.2:c.887T>C , LRG_287t1:c.887T>C	NP_000209.2:p.Phe296Ser
NM_181798.1:c.506T>C , LRG_287t2:c.506T>C	NP_861463.1:p.Phe169Ser
NM_000218.3:c.887T>C MANE Select	NP_000209.2:p.Phe296Ser