Canonical Allele Identifier: CA1948242706
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2572052C= , CM000673.2:g.2572052C= GRCh38
NC_000011.9:g.2593282C= , CM000673.1:g.2593282C= GRCh37
NC_000011.8:g.2549858C= NCBI36
NG_008935.1:g.132062C= , LRG_287:g.132062C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.462C= ENSP00000434560.2:p.Val154=
ENST00000646564.2:c.478-11383C= ENSP00000495806.2:n.478-11383C=
ENST00000155840.12:c.723C= MANE Select ENSP00000155840.2:p.Val241=
ENST00000335475.6:c.342C= ENSP00000334497.5:p.Val114=
ENST00000646564.1:c.124-11383C= ENSP00000495806.1:n.124-11383C=
ENST00000155840.9:c.723C= ENSP00000155840.2:p.Val241=
ENST00000335475.5:c.342C= ENSP00000334497.5:p.Val114=
ENST00000496887.6:c.462C= ENSP00000434560.1:p.Val154=
NM_000218.2:c.723C= , LRG_287t1:c.723C= NP_000209.2:p.Val241=
NM_181798.1:c.342C= , LRG_287t2:c.342C= NP_861463.1:p.Val114=
NM_000218.3:c.723C= MANE Select NP_000209.2:p.Val241=