Canonical Allele Identifier: CA379479647

Gene: KCNQ1 KCNQ1OT1

Linked Data

• MyVariant Identifiers: chr11:g.2683262C>G (hg19) ; chr11:g.2662032C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2662032C>G , CM000673.2:g.2662032C>G	GRCh38
NC_000011.9:g.2683262C>G , CM000673.1:g.2683262C>G	GRCh37
NC_000011.8:g.2639838C>G	NCBI36
NG_008935.1:g.222042C>G , LRG_287:g.222042C>G
NG_016178.2:g.42967G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.1108C>G (KCNQ1)	ENSP00000434560.2:p.Leu370Val
ENST00000646564.2:c.925C>G (KCNQ1)	ENSP00000495806.2:p.Leu309Val
ENST00000155840.12:c.1465C>G (KCNQ1) MANE Select	ENSP00000155840.2:p.Leu489Val
ENST00000335475.6:c.1084C>G (KCNQ1)	ENSP00000334497.5:p.Leu362Val
ENST00000646564.1:c.571C>G (KCNQ1)	ENSP00000495806.1:p.Leu191Val
ENST00000155840.9:c.1465C>G (KCNQ1)	ENSP00000155840.2:p.Leu489Val
ENST00000335475.5:c.1084C>G (KCNQ1)	ENSP00000334497.5:p.Leu362Val
NM_000218.2:c.1465C>G , LRG_287t1:c.1465C>G (KCNQ1)	NP_000209.2:p.Leu489Val
NM_181798.1:c.1084C>G , LRG_287t2:c.1084C>G (KCNQ1)	NP_861463.1:p.Leu362Val
NR_002728.3:n.37967G>C (KCNQ1OT1)
NM_000218.3:c.1465C>G (KCNQ1) MANE Select	NP_000209.2:p.Leu489Val