Canonical Allele Identifier: CA379479655

Gene: KCNQ1 KCNQ1OT1

Linked Data

• dbSNP Id: rs1849967442
• MyVariant Identifiers: chr11:g.2683263T>G (hg19) ; chr11:g.2662033T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2662033T>G , CM000673.2:g.2662033T>G	GRCh38
NC_000011.9:g.2683263T>G , CM000673.1:g.2683263T>G	GRCh37
NC_000011.8:g.2639839T>G	NCBI36
NG_008935.1:g.222043T>G , LRG_287:g.222043T>G
NG_016178.2:g.42966A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1109T>G (KCNQ1)	ENSP00000434560.2:p.Leu370Arg
ENST00000646564.2:c.926T>G (KCNQ1)	ENSP00000495806.2:p.Leu309Arg
ENST00000155840.12:c.1466T>G (KCNQ1) MANE Select	ENSP00000155840.2:p.Leu489Arg
ENST00000335475.6:c.1085T>G (KCNQ1)	ENSP00000334497.5:p.Leu362Arg
ENST00000646564.1:c.572T>G (KCNQ1)	ENSP00000495806.1:p.Leu191Arg
ENST00000155840.9:c.1466T>G (KCNQ1)	ENSP00000155840.2:p.Leu489Arg
ENST00000335475.5:c.1085T>G (KCNQ1)	ENSP00000334497.5:p.Leu362Arg
NM_000218.2:c.1466T>G , LRG_287t1:c.1466T>G (KCNQ1)	NP_000209.2:p.Leu489Arg
NM_181798.1:c.1085T>G , LRG_287t2:c.1085T>G (KCNQ1)	NP_861463.1:p.Leu362Arg
NR_002728.3:n.37966A>C (KCNQ1OT1)
NM_000218.3:c.1466T>G (KCNQ1) MANE Select	NP_000209.2:p.Leu489Arg