Canonical Allele Identifier: CA1143559620
Gene: KCNQ4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40838475C= , CM000663.2:g.40838475C= GRCh38
NC_000001.10:g.41304147C= , CM000663.1:g.41304147C= GRCh37
NC_000001.9:g.41076734C= NCBI36
NG_008139.1:g.59464C=
NG_008139.2:g.59464C=
NG_008139.3:g.59689C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000347132.10:c.2040C= MANE Select ENSP00000262916.6:p.Ser680=
ENST00000347132.9:c.2040C= ENSP00000262916.6:p.Ser680=
ENST00000443478.3:c.1621C=
ENST00000506017.1:n.1359C=
ENST00000509682.6:c.1878C= ENSP00000423756.2:p.Ser626=
NM_004700.3:c.2040C= NP_004691.2:p.Ser680=
NM_172163.2:c.1878C= NP_751895.1:p.Ser626=
XM_017002792.1:c.1023C= XP_016858281.1:p.Ser341=
NM_004700.4:c.2040C= MANE Select NP_004691.2:p.Ser680=
NM_172163.3:c.1878C= NP_751895.1:p.Ser626=