Canonical Allele Identifier: CA379121369

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2549190G>C (hg19) ; chr11:g.2527960G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2527960G>C , CM000673.2:g.2527960G>C	GRCh38
NC_000011.9:g.2549190G>C , CM000673.1:g.2549190G>C	GRCh37
NC_000011.8:g.2505766G>C	NCBI36
NG_008935.1:g.87970G>C , LRG_287:g.87970G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000380776.5:n.216G>C
ENST00000496887.7:c.158G>C	ENSP00000434560.2:p.Ser53Thr
ENST00000646564.2:c.419G>C	ENSP00000495806.2:p.Ser140Thr
ENST00000155840.12:c.419G>C MANE Select	ENSP00000155840.2:p.Ser140Thr
ENST00000335475.6:c.38G>C	ENSP00000334497.5:p.Ser13Thr
ENST00000646564.1:c.65G>C	ENSP00000495806.1:p.Ser22Thr
ENST00000155840.9:c.419G>C	ENSP00000155840.2:p.Ser140Thr
ENST00000335475.5:c.38G>C	ENSP00000334497.5:p.Ser13Thr
ENST00000345015.4:n.288G>C
ENST00000380776.4:c.209G>C	ENSP00000370153.4:p.Ser70Thr
ENST00000496887.6:c.158G>C	ENSP00000434560.1:p.Ser53Thr
NM_000218.2:c.419G>C , LRG_287t1:c.419G>C	NP_000209.2:p.Ser140Thr
NM_181798.1:c.38G>C , LRG_287t2:c.38G>C	NP_861463.1:p.Ser13Thr
NM_000218.3:c.419G>C MANE Select	NP_000209.2:p.Ser140Thr