Canonical Allele Identifier: CA10582882

Gene: KCNQ1

Linked Data

• ClinVar Variation Id: 237228
• ClinVar RCV Id: RCV000229159
• dbSNP Id: rs120074178
• MyVariant Identifiers: chr11:g.2591949G>C (hg19) ; chr11:g.2570719G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2570719G>C , CM000673.2:g.2570719G>C	GRCh38
NC_000011.9:g.2591949G>C , CM000673.1:g.2591949G>C	GRCh37
NC_000011.8:g.2548525G>C	NCBI36
NG_008935.1:g.130729G>C , LRG_287:g.130729G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.308G>C	ENSP00000434560.2:p.Arg103Pro
ENST00000646564.2:c.478-12716G>C	ENSP00000495806.2:n.478-12716G>C
ENST00000155840.12:c.569G>C MANE Select	ENSP00000155840.2:p.Arg190Pro
ENST00000335475.6:c.188G>C	ENSP00000334497.5:p.Arg63Pro
ENST00000646564.1:c.124-12716G>C	ENSP00000495806.1:n.124-12716G>C
ENST00000155840.9:c.569G>C	ENSP00000155840.2:p.Arg190Pro
ENST00000335475.5:c.188G>C	ENSP00000334497.5:p.Arg63Pro
ENST00000496887.6:c.308G>C	ENSP00000434560.1:p.Arg103Pro
NM_000218.2:c.569G>C , LRG_287t1:c.569G>C	NP_000209.2:p.Arg190Pro
NM_181798.1:c.188G>C , LRG_287t2:c.188G>C	NP_861463.1:p.Arg63Pro
NM_000218.3:c.569G>C MANE Select	NP_000209.2:p.Arg190Pro