Canonical Allele Identifier: CA379133094
Gene: KCNQ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2583518T>G , CM000673.2:g.2583518T>G GRCh38
NC_000011.9:g.2604748T>G , CM000673.1:g.2604748T>G GRCh37
NC_000011.8:g.2561324T>G NCBI36
NG_008935.1:g.143528T>G , LRG_287:g.143528T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.744T>G ENSP00000434560.2:p.Phe248Leu
ENST00000646564.2:c.561T>G ENSP00000495806.2:p.Phe187Leu
ENST00000155840.12:c.1005T>G MANE Select ENSP00000155840.2:p.Phe335Leu
ENST00000335475.6:c.624T>G ENSP00000334497.5:p.Phe208Leu
ENST00000646564.1:c.207T>G ENSP00000495806.1:p.Phe69Leu
ENST00000155840.9:c.1005T>G ENSP00000155840.2:p.Phe335Leu
ENST00000335475.5:c.624T>G ENSP00000334497.5:p.Phe208Leu
NM_000218.2:c.1005T>G , LRG_287t1:c.1005T>G NP_000209.2:p.Phe335Leu
NM_181798.1:c.624T>G , LRG_287t2:c.624T>G NP_861463.1:p.Phe208Leu
NM_000218.3:c.1005T>G MANE Select NP_000209.2:p.Phe335Leu