Canonical Allele Identifier: CA379479678

Gene: KCNQ1 KCNQ1OT1

Linked Data

• MyVariant Identifiers: chr11:g.2683267C>A (hg19) ; chr11:g.2662037C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2662037C>A , CM000673.2:g.2662037C>A	GRCh38
NC_000011.9:g.2683267C>A , CM000673.1:g.2683267C>A	GRCh37
NC_000011.8:g.2639843C>A	NCBI36
NG_008935.1:g.222047C>A , LRG_287:g.222047C>A
NG_016178.2:g.42962G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000496887.7:c.1113C>A (KCNQ1)	ENSP00000434560.2:p.Asp371Glu
ENST00000646564.2:c.930C>A (KCNQ1)	ENSP00000495806.2:p.Asp310Glu
ENST00000155840.12:c.1470C>A (KCNQ1) MANE Select	ENSP00000155840.2:p.Asp490Glu
ENST00000335475.6:c.1089C>A (KCNQ1)	ENSP00000334497.5:p.Asp363Glu
ENST00000646564.1:c.576C>A (KCNQ1)	ENSP00000495806.1:p.Asp192Glu
ENST00000155840.9:c.1470C>A (KCNQ1)	ENSP00000155840.2:p.Asp490Glu
ENST00000335475.5:c.1089C>A (KCNQ1)	ENSP00000334497.5:p.Asp363Glu
NM_000218.2:c.1470C>A , LRG_287t1:c.1470C>A (KCNQ1)	NP_000209.2:p.Asp490Glu
NM_181798.1:c.1089C>A , LRG_287t2:c.1089C>A (KCNQ1)	NP_861463.1:p.Asp363Glu
NR_002728.3:n.37962G>T (KCNQ1OT1)
NM_000218.3:c.1470C>A (KCNQ1) MANE Select	NP_000209.2:p.Asp490Glu