Canonical Allele Identifier: CA2525181686
Gene: KCNQ1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2570624G>A , CM000673.2:g.2570624G>A GRCh38
NC_000011.9:g.2591854G>A , CM000673.1:g.2591854G>A GRCh37
NC_000011.8:g.2548430G>A NCBI36
NG_008935.1:g.130634G>A , LRG_287:g.130634G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.217-4G>A ENSP00000434560.2:n.217-4G>A
ENST00000646564.2:c.478-12811G>A ENSP00000495806.2:n.478-12811G>A
ENST00000155840.12:c.478-4G>A MANE Select ENSP00000155840.2:n.478-4G>A
ENST00000335475.6:c.97-4G>A ENSP00000334497.5:n.97-4G>A
ENST00000646564.1:c.124-12811G>A ENSP00000495806.1:n.124-12811G>A
ENST00000155840.9:c.478-4G>A ENSP00000155840.2:n.478-4G>A
ENST00000335475.5:c.97-4G>A ENSP00000334497.5:n.97-4G>A
ENST00000496887.6:c.217-4G>A ENSP00000434560.1:n.217-4G>A
NM_000218.2:c.478-4G>A , LRG_287t1:c.478-4G>A NP_000209.2:n.478-4G>A
NM_181798.1:c.97-4G>A , LRG_287t2:c.97-4G>A NP_861463.1:n.97-4G>A
NM_000218.3:c.478-4G>A MANE Select NP_000209.2:n.478-4G>A
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