Canonical Allele Identifier: CA645523677
Gene: KCNQ4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40784110del , CM000663.2:g.40784110del GRCh38
NC_000001.10:g.41249782del , CM000663.1:g.41249782del GRCh37
NC_000001.9:g.41022369del NCBI36
NG_008139.1:g.5099del
NG_008139.2:g.5099del
NG_008139.3:g.5324del

Transcript Alleles

HGVS Amino-acid Change
ENST00000347132.10:c.17del MANE Select ENSP00000262916.6:p.Pro6ArgfsTer18
ENST00000347132.9:c.17del ENSP00000262916.6:p.Pro6ArgfsTer18
ENST00000509682.6:c.17del ENSP00000423756.2:p.Pro6ArgfsTer18
NM_004700.3:c.17del NP_004691.2:p.Pro6ArgfsTer18
NM_172163.2:c.17del NP_751895.1:p.Pro6ArgfsTer18
XM_011542417.1:c.17del XP_011540719.1:p.Pro6ArgfsTer18
XM_011542418.1:c.17del XP_011540720.1:p.Pro6ArgfsTer18
XM_011542419.1:c.17del XP_011540721.1:p.Pro6ArgfsTer18
XM_011542420.1:c.17del XP_011540722.1:p.Pro6ArgfsTer18
XR_946798.1:n.23del
XR_946799.1:n.23del
XR_946800.1:n.23del
NM_004700.4:c.17del MANE Select NP_004691.2:p.Pro6ArgfsTer18
NM_172163.3:c.17del NP_751895.1:p.Pro6ArgfsTer18