Canonical Allele Identifier: CA472236326

Gene: KCNQ1 KCNQ1OT1

Linked Data

• MyVariant Identifiers: chr11:g.2683294C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2662064C>A , CM000673.2:g.2662064C>A	GRCh38
NC_000011.9:g.2683294C>A , CM000673.1:g.2683294C>A	GRCh37
NC_000011.8:g.2639870C>A	NCBI36
NG_008935.1:g.222074C>A , LRG_287:g.222074C>A
NG_016178.2:g.42935G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1140C>A (KCNQ1)	ENSP00000434560.2:p.Pro380=
ENST00000646564.2:c.957C>A (KCNQ1)	ENSP00000495806.2:p.Pro319=
ENST00000155840.12:c.1497C>A (KCNQ1) MANE Select	ENSP00000155840.2:p.Pro499=
ENST00000335475.6:c.1116C>A (KCNQ1)	ENSP00000334497.5:p.Pro372=
ENST00000646564.1:c.603C>A (KCNQ1)	ENSP00000495806.1:p.Pro201=
ENST00000155840.9:c.1497C>A (KCNQ1)	ENSP00000155840.2:p.Pro499=
ENST00000335475.5:c.1116C>A (KCNQ1)	ENSP00000334497.5:p.Pro372=
NM_000218.2:c.1497C>A , LRG_287t1:c.1497C>A (KCNQ1)	NP_000209.2:p.Pro499=
NM_181798.1:c.1116C>A , LRG_287t2:c.1116C>A (KCNQ1)	NP_861463.1:p.Pro372=
NR_002728.3:n.37935G>T (KCNQ1OT1)
NM_000218.3:c.1497C>A (KCNQ1) MANE Select	NP_000209.2:p.Pro499=