Canonical Allele Identifier: CA379134739

Gene: KCNQ1

Linked Data

• ClinVar Variation Id: 3075342
• ClinVar RCV Id: RCV004015868
• MyVariant Identifiers: chr11:g.2608850G>C (hg19) ; chr11:g.2587620G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2587620G>C , CM000673.2:g.2587620G>C	GRCh38
NC_000011.9:g.2608850G>C , CM000673.1:g.2608850G>C	GRCh37
NC_000011.8:g.2565426G>C	NCBI36
NG_008935.1:g.147630G>C , LRG_287:g.147630G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.822G>C	ENSP00000434560.2:p.Lys274Asn
ENST00000646564.2:c.639G>C	ENSP00000495806.2:p.Lys213Asn
ENST00000155840.12:c.1179G>C MANE Select	ENSP00000155840.2:p.Lys393Asn
ENST00000335475.6:c.798G>C	ENSP00000334497.5:p.Lys266Asn
ENST00000646564.1:c.285G>C	ENSP00000495806.1:p.Lys95Asn
ENST00000155840.9:c.1179G>C	ENSP00000155840.2:p.Lys393Asn
ENST00000335475.5:c.798G>C	ENSP00000334497.5:p.Lys266Asn
NM_000218.2:c.1179G>C , LRG_287t1:c.1179G>C	NP_000209.2:p.Lys393Asn
NM_181798.1:c.798G>C , LRG_287t2:c.798G>C	NP_861463.1:p.Lys266Asn
NM_000218.3:c.1179G>C MANE Select	NP_000209.2:p.Lys393Asn