Canonical Allele Identifier: CA472038403
Gene: KCNQ1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.2604676C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2583446C>T , CM000673.2:g.2583446C>T GRCh38
NC_000011.9:g.2604676C>T , CM000673.1:g.2604676C>T GRCh37
NC_000011.8:g.2561252C>T NCBI36
NG_008935.1:g.143456C>T , LRG_287:g.143456C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.672C>T ENSP00000434560.2:p.Thr224=
ENST00000646564.2:c.489C>T ENSP00000495806.2:p.Thr163=
ENST00000155840.12:c.933C>T MANE Select ENSP00000155840.2:p.Thr311=
ENST00000335475.6:c.552C>T ENSP00000334497.5:p.Thr184=
ENST00000646564.1:c.135C>T ENSP00000495806.1:p.Thr45=
ENST00000155840.9:c.933C>T ENSP00000155840.2:p.Thr311=
ENST00000335475.5:c.552C>T ENSP00000334497.5:p.Thr184=
NM_000218.2:c.933C>T , LRG_287t1:c.933C>T NP_000209.2:p.Thr311=
NM_181798.1:c.552C>T , LRG_287t2:c.552C>T NP_861463.1:p.Thr184=
NM_000218.3:c.933C>T MANE Select NP_000209.2:p.Thr311=