Canonical Allele Identifier: CA379134671
Gene: KCNQ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2587586A>G , CM000673.2:g.2587586A>G GRCh38
NC_000011.9:g.2608816A>G , CM000673.1:g.2608816A>G GRCh37
NC_000011.8:g.2565392A>G NCBI36
NG_008935.1:g.147596A>G , LRG_287:g.147596A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.788A>G ENSP00000434560.2:p.Tyr263Cys
ENST00000646564.2:c.605A>G ENSP00000495806.2:p.Tyr202Cys
ENST00000155840.12:c.1145A>G MANE Select ENSP00000155840.2:p.Tyr382Cys
ENST00000335475.6:c.764A>G ENSP00000334497.5:p.Tyr255Cys
ENST00000646564.1:c.251A>G ENSP00000495806.1:p.Tyr84Cys
ENST00000155840.9:c.1145A>G ENSP00000155840.2:p.Tyr382Cys
ENST00000335475.5:c.764A>G ENSP00000334497.5:p.Tyr255Cys
NM_000218.2:c.1145A>G , LRG_287t1:c.1145A>G NP_000209.2:p.Tyr382Cys
NM_181798.1:c.764A>G , LRG_287t2:c.764A>G NP_861463.1:p.Tyr255Cys
NM_000218.3:c.1145A>G MANE Select NP_000209.2:p.Tyr382Cys