Canonical Allele Identifier: CA2840405426

Gene: KCNQ1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2572821dup , CM000673.2:g.2572821dup	GRCh38
NC_000011.9:g.2594051dup , CM000673.1:g.2594051dup	GRCh37
NC_000011.8:g.2550627dup	NCBI36
NG_008935.1:g.132831dup , LRG_287:g.132831dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.520-25dup	ENSP00000434560.2:n.520-25dup
ENST00000646564.2:c.478-10614dup	ENSP00000495806.2:n.478-10614dup
ENST00000155840.12:c.781-25dup MANE Select	ENSP00000155840.2:n.781-25dup
ENST00000335475.6:c.400-25dup	ENSP00000334497.5:n.400-25dup
ENST00000646564.1:c.124-10614dup	ENSP00000495806.1:n.124-10614dup
ENST00000155840.9:c.781-25dup	ENSP00000155840.2:n.781-25dup
ENST00000335475.5:c.400-25dup	ENSP00000334497.5:n.400-25dup
ENST00000496887.6:c.520-25dup	ENSP00000434560.1:n.520-25dup
NM_000218.2:c.781-25dup , LRG_287t1:c.781-25dup	NP_000209.2:n.781-25dup
NM_181798.1:c.400-25dup , LRG_287t2:c.400-25dup	NP_861463.1:n.400-25dup
NM_000218.3:c.781-25dup MANE Select	NP_000209.2:n.781-25dup