Canonical Allele Identifier: CA472037864
Gene: KCNQ1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.2591941C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2570711C>T , CM000673.2:g.2570711C>T GRCh38
NC_000011.9:g.2591941C>T , CM000673.1:g.2591941C>T GRCh37
NC_000011.8:g.2548517C>T NCBI36
NG_008935.1:g.130721C>T , LRG_287:g.130721C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.300C>T ENSP00000434560.2:p.Leu100=
ENST00000646564.2:c.478-12724C>T ENSP00000495806.2:n.478-12724C>T
ENST00000155840.12:c.561C>T MANE Select ENSP00000155840.2:p.Leu187=
ENST00000335475.6:c.180C>T ENSP00000334497.5:p.Leu60=
ENST00000646564.1:c.124-12724C>T ENSP00000495806.1:n.124-12724C>T
ENST00000155840.9:c.561C>T ENSP00000155840.2:p.Leu187=
ENST00000335475.5:c.180C>T ENSP00000334497.5:p.Leu60=
ENST00000496887.6:c.300C>T ENSP00000434560.1:p.Leu100=
NM_000218.2:c.561C>T , LRG_287t1:c.561C>T NP_000209.2:p.Leu187=
NM_181798.1:c.180C>T , LRG_287t2:c.180C>T NP_861463.1:p.Leu60=
NM_000218.3:c.561C>T MANE Select NP_000209.2:p.Leu187=