Canonical Allele Identifier: CA1948243126
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2572782G= , CM000673.2:g.2572782G= GRCh38
NC_000011.9:g.2594012G= , CM000673.1:g.2594012G= GRCh37
NC_000011.8:g.2550588G= NCBI36
NG_008935.1:g.132792G= , LRG_287:g.132792G=

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.520-64G= ENSP00000434560.2:n.520-64G=
ENST00000646564.2:c.478-10653G= ENSP00000495806.2:n.478-10653G=
ENST00000155840.12:c.781-64G= MANE Select ENSP00000155840.2:n.781-64G=
ENST00000335475.6:c.400-64G= ENSP00000334497.5:n.400-64G=
ENST00000646564.1:c.124-10653G= ENSP00000495806.1:n.124-10653G=
ENST00000155840.9:c.781-64G= ENSP00000155840.2:n.781-64G=
ENST00000335475.5:c.400-64G= ENSP00000334497.5:n.400-64G=
ENST00000496887.6:c.520-64G= ENSP00000434560.1:n.520-64G=
NM_000218.2:c.781-64G= , LRG_287t1:c.781-64G= NP_000209.2:n.781-64G=
NM_181798.1:c.400-64G= , LRG_287t2:c.400-64G= NP_861463.1:n.400-64G=
NM_000218.3:c.781-64G= MANE Select NP_000209.2:n.781-64G=