Canonical Allele Identifier: CA1149151140

Gene: KCNQ4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40819465_40819469delinsGGGGG , CM000663.2:g.40819465_40819469delinsGGGGG	GRCh38
NC_000001.10:g.41285137_41285141delinsGGGGG , CM000663.1:g.41285137_41285141delinsGGGGG	GRCh37
NC_000001.9:g.41057724_41057728delinsGGGGG	NCBI36
NG_008139.1:g.40454_40458delinsGGGGG
NG_008139.2:g.40454_40458delinsGGGGG
NG_008139.3:g.40679_40683delinsGGGGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000347132.10:c.827_831delinsGGGGG MANE Select	ENSP00000262916.6:p.Trp276=
ENST00000347132.9:c.827_831delinsGGGGG	ENSP00000262916.6:p.Trp276=
ENST00000443478.3:c.513_517delinsGGGGG
ENST00000506017.1:n.146_150delinsGGGGG
ENST00000509682.6:c.827_831delinsGGGGG	ENSP00000423756.2:p.Trp276=
NM_004700.3:c.827_831delinsGGGGG	NP_004691.2:p.Trp276=
NM_172163.2:c.827_831delinsGGGGG	NP_751895.1:p.Trp276=
XM_011542417.1:c.827_831delinsGGGGG	XP_011540719.1:p.Trp276=
XM_011542418.1:c.827_831delinsGGGGG	XP_011540720.1:p.Trp276=
XM_011542419.1:c.827_831delinsGGGGG	XP_011540721.1:p.Trp276=
XM_011542420.1:c.827_831delinsGGGGG	XP_011540722.1:p.Trp276=
XR_946798.1:n.833_837delinsGGGGG
XR_946799.1:n.833_837delinsGGGGG
XR_946800.1:n.833_837delinsGGGGG
XM_017002792.1:c.-191_-187delinsGGGGG	XP_016858281.1:n.-191_-187delinsGGGGG
NM_004700.4:c.827_831delinsGGGGG MANE Select	NP_004691.2:p.Trp276=
NM_172163.3:c.827_831delinsGGGGG	NP_751895.1:p.Trp276=