Canonical Allele Identifier: CA1141188915
Gene: KCNQ4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40784304_40784317delinsCAGCGCTCCTCGGC , CM000663.2:g.40784304_40784317delinsCAGCGCTCCTCGGC GRCh38
NC_000001.10:g.41249976_41249989delinsCAGCGCTCCTCGGC , CM000663.1:g.41249976_41249989delinsCAGCGCTCCTCGGC GRCh37
NC_000001.9:g.41022563_41022576delinsCAGCGCTCCTCGGC NCBI36
NG_008139.1:g.5293_5306delinsCAGCGCTCCTCGGC
NG_008139.2:g.5293_5306delinsCAGCGCTCCTCGGC
NG_008139.3:g.5518_5531delinsCAGCGCTCCTCGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000347132.10:c.211_224delinsCAGCGCTCCTCGGC MANE Select ENSP00000262916.6:p.Gln71=
ENST00000347132.9:c.211_224delinsCAGCGCTCCTCGGC ENSP00000262916.6:p.Gln71=
ENST00000509682.6:c.211_224delinsCAGCGCTCCTCGGC ENSP00000423756.2:p.Gln71=
NM_004700.3:c.211_224delinsCAGCGCTCCTCGGC NP_004691.2:p.Gln71=
NM_172163.2:c.211_224delinsCAGCGCTCCTCGGC NP_751895.1:p.Gln71=
XM_011542417.1:c.211_224delinsCAGCGCTCCTCGGC XP_011540719.1:p.Gln71=
XM_011542418.1:c.211_224delinsCAGCGCTCCTCGGC XP_011540720.1:p.Gln71=
XM_011542419.1:c.211_224delinsCAGCGCTCCTCGGC XP_011540721.1:p.Gln71=
XM_011542420.1:c.211_224delinsCAGCGCTCCTCGGC XP_011540722.1:p.Gln71=
XR_946798.1:n.217_230delinsCAGCGCTCCTCGGC
XR_946799.1:n.217_230delinsCAGCGCTCCTCGGC
XR_946800.1:n.217_230delinsCAGCGCTCCTCGGC
NM_004700.4:c.211_224delinsCAGCGCTCCTCGGC MANE Select NP_004691.2:p.Gln71=
NM_172163.3:c.211_224delinsCAGCGCTCCTCGGC NP_751895.1:p.Gln71=