Canonical Allele Identifier: CA2645137075
Gene: KCNQ4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40819496del , CM000663.2:g.40819496del GRCh38
NC_000001.10:g.41285168del , CM000663.1:g.41285168del GRCh37
NC_000001.9:g.41057755del NCBI36
NG_008139.1:g.40485del
NG_008139.2:g.40485del
NG_008139.3:g.40710del

Transcript Alleles

HGVS Amino-acid Change
ENST00000347132.10:c.834+24del MANE Select ENSP00000262916.6:n.834+24del
ENST00000347132.9:c.834+24del ENSP00000262916.6:n.834+24del
ENST00000443478.3:c.520+24del
ENST00000506017.1:n.153+24del
ENST00000509682.6:c.834+24del ENSP00000423756.2:n.834+24del
NM_004700.3:c.834+24del NP_004691.2:n.834+24del
NM_172163.2:c.834+24del NP_751895.1:n.834+24del
XM_011542417.1:c.834+24del XP_011540719.1:n.834+24del
XM_011542418.1:c.834+24del XP_011540720.1:n.834+24del
XM_011542419.1:c.834+24del XP_011540721.1:n.834+24del
XM_011542420.1:c.834+24del XP_011540722.1:n.834+24del
XR_946798.1:n.840+24del
XR_946799.1:n.840+24del
XR_946800.1:n.840+24del
XM_017002792.1:c.-184+24del XP_016858281.1:n.-184+24del
NM_004700.4:c.834+24del MANE Select NP_004691.2:n.834+24del
NM_172163.3:c.834+24del NP_751895.1:n.834+24del