Canonical Allele Identifier: CA1948224243
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2583240G= , CM000673.2:g.2583240G= GRCh38
NC_000011.9:g.2604470G= , CM000673.1:g.2604470G= GRCh37
NC_000011.8:g.2561046G= NCBI36
NG_008935.1:g.143250G= , LRG_287:g.143250G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.661-195G= ENSP00000434560.2:n.661-195G=
ENST00000646564.2:c.478-195G= ENSP00000495806.2:n.478-195G=
ENST00000155840.12:c.922-195G= MANE Select ENSP00000155840.2:n.922-195G=
ENST00000335475.6:c.541-195G= ENSP00000334497.5:n.541-195G=
ENST00000646564.1:c.124-195G= ENSP00000495806.1:n.124-195G=
ENST00000155840.9:c.922-195G= ENSP00000155840.2:n.922-195G=
ENST00000335475.5:c.541-195G= ENSP00000334497.5:n.541-195G=
NM_000218.2:c.922-195G= , LRG_287t1:c.922-195G= NP_000209.2:n.922-195G=
NM_181798.1:c.541-195G= , LRG_287t2:c.541-195G= NP_861463.1:n.541-195G=
NM_000218.3:c.922-195G= MANE Select NP_000209.2:n.922-195G=