Canonical Allele Identifier: CA1164531191

Gene: KCNQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40784302_40784303delinsGC , CM000663.2:g.40784302_40784303delinsGC	GRCh38
NC_000001.10:g.41249974_41249975delinsGC , CM000663.1:g.41249974_41249975delinsGC	GRCh37
NC_000001.9:g.41022561_41022562delinsGC	NCBI36
NG_008139.1:g.5291_5292delinsGC
NG_008139.2:g.5291_5292delinsGC
NG_008139.3:g.5516_5517delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347132.10:c.209_210delinsGC MANE Select	ENSP00000262916.6:p.Gly70=
ENST00000347132.9:c.209_210delinsGC	ENSP00000262916.6:p.Gly70=
ENST00000509682.6:c.209_210delinsGC	ENSP00000423756.2:p.Gly70=
NM_004700.3:c.209_210delinsGC	NP_004691.2:p.Gly70=
NM_172163.2:c.209_210delinsGC	NP_751895.1:p.Gly70=
XM_011542417.1:c.209_210delinsGC	XP_011540719.1:p.Gly70=
XM_011542418.1:c.209_210delinsGC	XP_011540720.1:p.Gly70=
XM_011542419.1:c.209_210delinsGC	XP_011540721.1:p.Gly70=
XM_011542420.1:c.209_210delinsGC	XP_011540722.1:p.Gly70=
XR_946798.1:n.215_216delinsGC
XR_946799.1:n.215_216delinsGC
XR_946800.1:n.215_216delinsGC
NM_004700.4:c.209_210delinsGC MANE Select	NP_004691.2:p.Gly70=
NM_172163.3:c.209_210delinsGC	NP_751895.1:p.Gly70=