Canonical Allele Identifier: CA008421

Gene: KCNQ1

Linked Data

• ClinVar Variation Id: 67110
• ClinVar RCV Id: RCV000057773
• dbSNP Id: rs199473461
• MyVariant Identifiers: chr11:g.2594124T>C (hg19) ; chr11:g.2572894T>C (hg38)
• PubMed: PMID:19716085 ; PMID:22581653

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2572894T>C , CM000673.2:g.2572894T>C	GRCh38
NC_000011.9:g.2594124T>C , CM000673.1:g.2594124T>C	GRCh37
NC_000011.8:g.2550700T>C	NCBI36
NG_008935.1:g.132904T>C , LRG_287:g.132904T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.568T>C	ENSP00000434560.2:p.Ser190Pro
ENST00000646564.2:c.478-10541T>C	ENSP00000495806.2:n.478-10541T>C
ENST00000155840.12:c.829T>C MANE Select	ENSP00000155840.2:p.Ser277Pro
ENST00000335475.6:c.448T>C	ENSP00000334497.5:p.Ser150Pro
ENST00000646564.1:c.124-10541T>C	ENSP00000495806.1:n.124-10541T>C
ENST00000155840.9:c.829T>C	ENSP00000155840.2:p.Ser277Pro
ENST00000335475.5:c.448T>C	ENSP00000334497.5:p.Ser150Pro
ENST00000496887.6:c.568T>C	ENSP00000434560.1:p.Ser190Pro
NM_000218.2:c.829T>C , LRG_287t1:c.829T>C	NP_000209.2:p.Ser277Pro
NM_181798.1:c.448T>C , LRG_287t2:c.448T>C	NP_861463.1:p.Ser150Pro
NM_000218.3:c.829T>C MANE Select	NP_000209.2:p.Ser277Pro