Canonical Allele Identifier: CA216335423

Gene: KCNQ1

Linked Data

• dbSNP Id: rs35494080
• MyVariant Identifiers: chr11:g.2610324_2610325insG (hg19) ; chr11:g.2589094_2589095insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2589098dup , CM000673.2:g.2589098dup	GRCh38
NC_000011.9:g.2610328dup , CM000673.1:g.2610328dup	GRCh37
NC_000011.8:g.2566904dup	NCBI36
NG_008935.1:g.149108dup , LRG_287:g.149108dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1036+244dup	ENSP00000434560.2:n.1036+244dup
ENST00000646564.2:c.853+244dup	ENSP00000495806.2:n.853+244dup
ENST00000155840.12:c.1393+244dup MANE Select	ENSP00000155840.2:n.1393+244dup
ENST00000335475.6:c.1012+244dup	ENSP00000334497.5:n.1012+244dup
ENST00000646564.1:c.499+244dup	ENSP00000495806.1:n.499+244dup
ENST00000155840.9:c.1393+244dup	ENSP00000155840.2:n.1393+244dup
ENST00000335475.5:c.1012+244dup	ENSP00000334497.5:n.1012+244dup
NM_000218.2:c.1393+244dup , LRG_287t1:c.1393+244dup	NP_000209.2:n.1393+244dup
NM_181798.1:c.1012+244dup , LRG_287t2:c.1012+244dup	NP_861463.1:n.1012+244dup
NM_000218.3:c.1393+244dup MANE Select	NP_000209.2:n.1393+244dup