Canonical Allele Identifier: CA379133854
Gene: KCNQ1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2585274C>G , CM000673.2:g.2585274C>G GRCh38
NC_000011.9:g.2606504C>G , CM000673.1:g.2606504C>G GRCh37
NC_000011.8:g.2563080C>G NCBI36
NG_008935.1:g.145284C>G , LRG_287:g.145284C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.771+1729C>G ENSP00000434560.2:n.771+1729C>G
ENST00000646564.2:c.588+1729C>G ENSP00000495806.2:n.588+1729C>G
ENST00000155840.12:c.1095C>G MANE Select ENSP00000155840.2:p.Asn365Lys
ENST00000335475.6:c.714C>G ENSP00000334497.5:p.Asn238Lys
ENST00000646564.1:c.234+1729C>G ENSP00000495806.1:n.234+1729C>G
ENST00000155840.9:c.1095C>G ENSP00000155840.2:p.Asn365Lys
ENST00000335475.5:c.714C>G ENSP00000334497.5:p.Asn238Lys
NM_000218.2:c.1095C>G , LRG_287t1:c.1095C>G NP_000209.2:p.Asn365Lys
NM_181798.1:c.714C>G , LRG_287t2:c.714C>G NP_861463.1:p.Asn238Lys
NM_000218.3:c.1095C>G MANE Select NP_000209.2:p.Asn365Lys