Canonical Allele Identifier: CA1164531129

Gene: KCNQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40784203_40784204delinsGC , CM000663.2:g.40784203_40784204delinsGC	GRCh38
NC_000001.10:g.41249875_41249876delinsGC , CM000663.1:g.41249875_41249876delinsGC	GRCh37
NC_000001.9:g.41022462_41022463delinsGC	NCBI36
NG_008139.1:g.5192_5193delinsGC
NG_008139.2:g.5192_5193delinsGC
NG_008139.3:g.5417_5418delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347132.10:c.110_111delinsGC MANE Select	ENSP00000262916.6:p.Gly37=
ENST00000347132.9:c.110_111delinsGC	ENSP00000262916.6:p.Gly37=
ENST00000509682.6:c.110_111delinsGC	ENSP00000423756.2:p.Gly37=
NM_004700.3:c.110_111delinsGC	NP_004691.2:p.Gly37=
NM_172163.2:c.110_111delinsGC	NP_751895.1:p.Gly37=
XM_011542417.1:c.110_111delinsGC	XP_011540719.1:p.Gly37=
XM_011542418.1:c.110_111delinsGC	XP_011540720.1:p.Gly37=
XM_011542419.1:c.110_111delinsGC	XP_011540721.1:p.Gly37=
XM_011542420.1:c.110_111delinsGC	XP_011540722.1:p.Gly37=
XR_946798.1:n.116_117delinsGC
XR_946799.1:n.116_117delinsGC
XR_946800.1:n.116_117delinsGC
NM_004700.4:c.110_111delinsGC MANE Select	NP_004691.2:p.Gly37=
NM_172163.3:c.110_111delinsGC	NP_751895.1:p.Gly37=