Canonical Allele Identifier: CA1948242734
Community Standard Title: NM_000218.3(KCNQ1):c.758C= (p.Ser253=)
Gene: KCNQ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2572087C= , CM000673.2:g.2572087C= GRCh38
NC_000011.9:g.2593317C= , CM000673.1:g.2593317C= GRCh37
NC_000011.8:g.2549893C= NCBI36
NG_008935.1:g.132097C= , LRG_287:g.132097C=

Transcript Alleles

HGVS Amino-acid Change
NM_000218.3:c.758C= MANE Select NP_000209.2:p.Ser253=
ENST00000155840.12:c.758C= MANE Select ENSP00000155840.2:p.Ser253=
NM_000218.2:c.758C= , LRG_287t1:c.758C= NP_000209.2:p.Ser253=
NM_181798.1:c.377C= , LRG_287t2:c.377C= NP_861463.1:p.Ser126=
ENST00000155840.9:c.758C= ENSP00000155840.2:p.Ser253=
ENST00000335475.5:c.377C= ENSP00000334497.5:p.Ser126=
ENST00000335475.6:c.377C= ENSP00000334497.5:p.Ser126=
ENST00000496887.6:c.497C= ENSP00000434560.1:p.Ser166=
ENST00000496887.7:c.497C= ENSP00000434560.2:p.Ser166=
ENST00000646564.1:c.124-11348C= ENSP00000495806.1:n.124-11348C=
ENST00000646564.2:c.478-11348C= ENSP00000495806.2:n.478-11348C=