Canonical Allele Identifier: CA1948236909
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2589094T= , CM000673.2:g.2589094T= GRCh38
NC_000011.9:g.2610324T= , CM000673.1:g.2610324T= GRCh37
NC_000011.8:g.2566900T= NCBI36
NG_008935.1:g.149104T= , LRG_287:g.149104T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.1036+240T= ENSP00000434560.2:n.1036+240T=
ENST00000646564.2:c.853+240T= ENSP00000495806.2:n.853+240T=
ENST00000155840.12:c.1393+240T= MANE Select ENSP00000155840.2:n.1393+240T=
ENST00000335475.6:c.1012+240T= ENSP00000334497.5:n.1012+240T=
ENST00000646564.1:c.499+240T= ENSP00000495806.1:n.499+240T=
ENST00000155840.9:c.1393+240T= ENSP00000155840.2:n.1393+240T=
ENST00000335475.5:c.1012+240T= ENSP00000334497.5:n.1012+240T=
NM_000218.2:c.1393+240T= , LRG_287t1:c.1393+240T= NP_000209.2:n.1393+240T=
NM_181798.1:c.1012+240T= , LRG_287t2:c.1012+240T= NP_861463.1:n.1012+240T=
NM_000218.3:c.1393+240T= MANE Select NP_000209.2:n.1393+240T=