Canonical Allele Identifier: CA2612004448

Gene: KCNQ1

Linked Data

• gnomAD v4: 11-2588905-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2588911dup , CM000673.2:g.2588911dup	GRCh38
NC_000011.9:g.2610141dup , CM000673.1:g.2610141dup	GRCh37
NC_000011.8:g.2566717dup	NCBI36
NG_008935.1:g.148921dup , LRG_287:g.148921dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.1036+57dup	ENSP00000434560.2:n.1036+57dup
ENST00000646564.2:c.853+57dup	ENSP00000495806.2:n.853+57dup
ENST00000155840.12:c.1393+57dup MANE Select	ENSP00000155840.2:n.1393+57dup
ENST00000335475.6:c.1012+57dup	ENSP00000334497.5:n.1012+57dup
ENST00000646564.1:c.499+57dup	ENSP00000495806.1:n.499+57dup
ENST00000155840.9:c.1393+57dup	ENSP00000155840.2:n.1393+57dup
ENST00000335475.5:c.1012+57dup	ENSP00000334497.5:n.1012+57dup
NM_000218.2:c.1393+57dup , LRG_287t1:c.1393+57dup	NP_000209.2:n.1393+57dup
NM_181798.1:c.1012+57dup , LRG_287t2:c.1012+57dup	NP_861463.1:n.1012+57dup
NM_000218.3:c.1393+57dup MANE Select	NP_000209.2:n.1393+57dup